Case report: autofluorescence imaging and phenotypic variance in a sibling pair with early-onset retinal dystrophy due to defective CRB1 function.

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Abstract

To phenotype two siblings with autosomal recessive early-onset retinal dystrophy due to CRB1 mutations.

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Journal

Journal ID (iso-abbrev): Curr. Eye Res.

Title: Current eye research

Publisher: Informa UK Limited

ISSN (Electronic): 1460-2202

ISSN (Print): 0271-3683

Publication date (Electronic): May 2009

Volume: 34

Issue: 5

Affiliations

[1 ] Bernard & Shirlee Brown Glaucoma Laboratory, Department of Ophthalmology, Columbia University, New York, New York, USA.

Article

Publisher Item ID: 910775367 Mid ID: NIHMS125938

DOI: 10.1080/02713680902859639

PMC ID: 2717950

PubMed ID: 19401883

SO-VID: 2620c2a8-6f97-4a0a-b2ae-79184b7f331f

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