X-linked centronuclear myopathy: Mapping the gene to Xq28 (Q28266328)

https://api.crossref.org/works/10.1016/0960-8966(91)90096-B

2 December 2022

main subject

centronuclear myopathy

1 reference

1 reference

https://api.crossref.org/works/10.1016/0960-8966(91)90096-B

2 December 2022

author name string

S. Liechti-Gallati

1

1 reference

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2 December 2022

B. Müller

2

1 reference

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2 December 2022

T. Grimm

3

1 reference

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2 December 2022

W. Kress

4

1 reference

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2 December 2022

C. Müller

5

1 reference

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2 December 2022

E. Boltshauser

6

1 reference

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2 December 2022

H. Moser

7

1 reference

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2 December 2022

S. Braga

8

1 reference

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full work available at URL

2 December 2022

language of work or name

English

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publication date

1991

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https://api.elsevier.com/content/article/PII:096089669190096B?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/0960-8966(91)90096-B

https://api.elsevier.com/content/article/PII:096089669190096B?httpAccept=text/plain

2 December 2022

1 reference

https://api.crossref.org/works/10.1016/0960-8966(91)90096-B

2 December 2022

published in

Neuromuscular Disorders

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volume

1

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issue

4

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page(s)

239-45

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cites work

Myotubular Myopathy

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1 reference

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X-linked myotubular myopathy with fatal neonatal asphyxia

2 December 2022

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1 reference

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Familial "myotubular" myopathy

2 December 2022

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Severe neonatal centronuclear (myotubular) myopathy: an X-linked recessive disorder

2 December 2022

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X-linked centronuclear myopathy as a cause of floppy baby

2 December 2022

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X-linked myotubular myopathy: clinical and pathological findings in a family

2 December 2022

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Severe neonatal asphyxia due to X-linked centronuclear myopathy

2 December 2022

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Centronuclear myopathy heterogeneity: Distinction of clinical types by myosin isoform patterns

2 December 2022

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X-linked recessive myotubular myopathy: I. Clinical and pathologic findings in a family

2 December 2022

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X-linked recessive myotubular myopathy: II. Muscle morphology and human myogenesis.

2 December 2022

11

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Congenital centronuclear (myotubular) myopathy. A clinical, pathological and genetic study in eight children

2 December 2022

12

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X linked neonatal centronuclear/myotubular myopathy: evidence for linkage to Xq28 DNA marker loci

2 December 2022

15

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https://api.crossref.org/works/10.1016/0960-8966(91)90096-B

X-linked myotubular myopathy: a linkage study

2 December 2022

16

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https://api.crossref.org/works/10.1016/0960-8966(91)90096-B

X linked neonatal myotubular myopathy: one recombination detected with four polymorphic DNA markers from Xq28

2 December 2022

17

1 reference

https://api.crossref.org/works/10.1016/0960-8966(91)90096-B

A linkage study of a large pedigree with X linked centronuclear myopathy

2 December 2022

18

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https://api.crossref.org/works/10.1016/0960-8966(91)90096-B

Characterization of the human factor VIII gene

2 December 2022

20

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https://api.crossref.org/works/10.1016/0960-8966(91)90096-B

Expression of active human factor VIII from recombinant DNA clones

2 December 2022

21

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Isolation of human glucose-6-phosphate dehydrogenase (G6PD) cDNA clones: primary structure of the protein and unusual 5' non-coding region

2 December 2022

22

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https://api.crossref.org/works/10.1016/0960-8966(91)90096-B

Molecular genetics of human color vision: the genes encoding blue, green, and red pigments

2 December 2022

23

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Linkage of adrenoleukodystrophy to a polymorphic DNA probe

2 December 2022

24

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Recombination between the factor VIII gene and the DXS52 locus gives the most probable genetic order as centromere-fra(X)-DXS15-DXS52-F8C-telomere

2 December 2022

26

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https://api.crossref.org/works/10.1016/0960-8966(91)90096-B

A 195-kb cosmid walk encompassing the human Xq28 color vision pigment genes

2 December 2022

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https://api.crossref.org/works/10.1016/0960-8966(91)90096-B

2 December 2022

Identifiers

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