X-linked juvenile retinoschisis: Clinical diagnosis, genetic analysis, and molecular mechanisms-Reference-Cited by-同舟云学术

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X-linked juvenile retinoschisis: Clinical diagnosis, genetic analysis, and molecular mechanisms

Published:2012-05 Issue:3 Volume:31 Page:195-212
ISSN:1350-9462
Container-title:Progress in Retinal and Eye Research
language:en
Short-container-title:Progress in Retinal and Eye Research

Author:

Molday Robert S.,Kellner Ulrich,Weber Bernhard H.F.

Funder

Foundation Fighting Blindness U.S., National Institutes of Health

Deutsche Forschungsgemeinschaft (DFG)

Macula Vision Research Foundation

Publisher

Elsevier BV

Subject

Sensory Systems,Ophthalmology

Reference206 articles.

1. Gene therapy restores vision in a canine model of childhood blindness;Acland;Nat. Genet.,2001

2. Restoration of cone vision in a mouse model of achromatopsia;Alexander;Nat. Med.,2007

3. Consanguineous marriage resulting in homozygous occurrence of X-linked retinoschisis in girls;Ali;Am. J. Ophthalmol.,2003

4. X-linked retinoschisis is closely linked to DXS41 and DXS16 but not DXS85;Alitalo;Clin. Genet.,1987

5. Biochemical and functional characterization of a novel neuron-glia adhesion molecule that is involved in neuronal migration;Antonicek;J. Cell Biol.,1987

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4. Early Developmental Characteristics and Features of a Three-Dimensional Retinal Organoid Model of X-Linked Juvenile Retinoschisis;International Journal of Molecular Sciences;2024-07-27

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