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Article

[TRPM1, a new gene implicated in congenital stationary night blindness].

Medecine sciences : M/S - 1 Mar 2010

Audo Isabelle, Sahel José-Alain, Bhattacharya Shomi, Zeitz Christina

Abstract excerpt

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Share to Calcium
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 20346272
DOI: 10.1051/medsci/2010263241

Genes

TRPM1

Provenance

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Related research

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Research trail→

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[TRPM1, a new gene implicated in congenital stationary night blindness].PMID 20346272Read ↗

Congenital Stationary Night Blindness due to Novel TRPM1 Gene Mutations in a Korean Patient.Semantic proximity Read ↗

TRPM1: new trends for an old TRP.Semantic proximity Read ↗

Unilateral cataract and congenital stationary night blindness in a child with novel variants in TRPM1.Semantic proximity Read ↗

Clinical and genetic findings in TRPM1-related congenital stationary night blindness.Semantic proximity Read ↗

A Mutation in SLC24A1 Implicated in Autosomal-Recessive Congenital Stationary Night BlindnessSemantic proximity Read ↗

Congenital stationary night blindness: mutation update and clinical variability.Semantic proximity Read ↗

Mutations in TRPM1 are a common cause of complete congenital stationary night blindness.Semantic proximity Read ↗

TRPM1 mutations are associated with the complete form of congenital stationary night blindness.Semantic proximity Read ↗

Congenital Stationary Night Blindness: Clinical and Genetic Features.Semantic proximity Read ↗

Congenital stationary night blindness: an update and review of the disease spectrum in Saudi Arabia.Semantic proximity Read ↗

Molecular profiling of complete congenital stationary night blindness: a pilot study on an Indian cohort.Semantic proximity Read ↗

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