Pages that link to "Q847057"
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The following pages link to retinitis pigmentosa (Q847057):
Displayed 50 items.
- disulfiram (Q409665) (← links)
- Josiah Jamison (Q1708638) (← links)
- Salvatore Cascio (Q2279307) (← links)
- Annalisa Minetti (Q2855108) (← links)
- Isaac Lidsky (Q4578334) (← links)
- Amar Latif (Q4740021) (← links)
- Chris McCausland (Q5107389) (← links)
- David S. Tatel (Q5239398) (← links)
- Gordon Gund (Q5585215) (← links)
- Mirhosseini–Holmes–Walton syndrome (Q6873219) (← links)
- retinal degeneration associated with rhodopsin mutations (Q7316761) (← links)
- Richard H. Bernstein (Q7326134) (← links)
- Richard O. Cowan (Q7328142) (← links)
- Ronan Pallier (Q7365480) (← links)
- Gerard Descarrega Puigdevall (Q16209062) (← links)
- CNGA1 (Q17907825) (← links)
- dystrophies primarily involving the retinal pigment epithelium (Q18554723) (← links)
- Exome sequencing identifies compound heterozygous mutations in CYP4V2 in a pedigree with retinitis pigmentosa (Q21090932) (← links)
- Midlife diagnosis of Refsum disease in siblings with retinitis pigmentosa -- the footprint is the clue: a case report (Q21093154) (← links)
- Cone rod dystrophies (Q21202953) (← links)
- Retinitis pigmentosa (Q21203028) (← links)
- Genes associated with retinitis pigmentosa and allied diseases are frequently mutated in the general population (Q21560782) (← links)
- Mechanisms of cell death in rhodopsin retinitis pigmentosa: implications for therapy (Q21710681) (← links)
- The retinitis pigmentosa GTPase regulator, RPGR, interacts with the delta subunit of rod cyclic GMP phosphodiesterase (Q22001446) (← links)
- Mutations in a gene encoding a new oxygen-regulated photoreceptor protein cause dominant retinitis pigmentosa (Q22010194) (← links)
- Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12) (Q22010603) (← links)
- Rebecca Redfern (Q24006298) (← links)
- Vitamin A and fish oils for retinitis pigmentosa (Q24201664) (← links)
- Vitamin A and fish oils for retinitis pigmentosa (Q24239931) (← links)
- Functional overlap between retinitis pigmentosa 2 protein and the tubulin-specific chaperone cofactor C (Q24292311) (← links)
- Protein 61K, encoded by a gene (PRPF31) linked to autosomal dominant retinitis pigmentosa, is required for U4/U6*U5 tri-snRNP formation and pre-mRNA splicing (Q24292373) (← links)
- Identification of a novel homozygous nonsense mutation in EYS in a Chinese family with autosomal recessive retinitis pigmentosa (Q24294725) (← links)
- A Mutation in ZNF513, a Putative Regulator of Photoreceptor Development, Causes Autosomal-Recessive Retinitis Pigmentosa (Q24297596) (← links)
- The retinitis pigmentosa protein RP2 links pericentriolar vesicle transport between the Golgi and the primary cilium (Q24297630) (← links)
- FAM161A, associated with retinitis pigmentosa, is a component of the cilia-basal body complex and interacts with proteins involved in ciliopathies (Q24297877) (← links)
- Mutations in the gene encoding the alpha subunit of the rod cGMP-gated channel in autosomal recessive retinitis pigmentosa (Q24303572) (← links)
- A three-base-pair deletion in the peripherin–RDS gene in one form of retinitis pigmentosa (Q24305284) (← links)
- A gene mutated in nephronophthisis and retinitis pigmentosa encodes a novel protein, nephroretinin, conserved in evolution (Q24305835) (← links)
- Two novel mutations in the EYS gene are possible major causes of autosomal recessive retinitis pigmentosa in the Japanese population (Q24306041) (← links)
- Identification of a PRPF4 loss-of-function variant that abrogates U4/U6.U5 tri-snRNP integration and is associated with retinitis pigmentosa (Q24306552) (← links)
- Discovery and functional analysis of a retinitis pigmentosa gene, C2ORF71 (Q24306827) (← links)
- RP1L1 variants are associated with a spectrum of inherited retinal diseases including retinitis pigmentosa and occult macular dystrophy (Q24307529) (← links)
- Recessive mutations in the gene encoding the tubby-like protein TULP1 in patients with retinitis pigmentosa (Q24309027) (← links)
- Missense mutations in a retinal pigment epithelium protein, bestrophin-1, cause retinitis pigmentosa (Q24310215) (← links)
- Identification of a 2 Mb human ortholog of Drosophila eyes shut/spacemaker that is mutated in patients with retinitis pigmentosa (Q24310728) (← links)
- A gene (SRPX) encoding a sushi-repeat-containing protein is deleted in patients with X-linked retinitis pigmentosa (Q24312152) (← links)
- Spectrum of mutations in the RPGR gene that are identified in 20% of families with X-linked retinitis pigmentosa (Q24313576) (← links)
- Dynamics of the rhomboid-like protein RHBDD2 expression in mouse retina and involvement of its human ortholog in retinitis pigmentosa (Q24314670) (← links)
- The retinitis pigmentosa 2 gene product is a GTPase-activating protein for Arf-like 3 (Q24315798) (← links)
- Localization in the human retina of the X-linked retinitis pigmentosa protein RP2, its homologue cofactor C and the RP2 interacting protein Arl3 (Q24316031) (← links)