A Null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosa

Journal article

Peer reviewed

Philip J Rosenfeld, Glenn S Cowley, Terri L McGee, Michael A Sandberg, Eliot L Berson and Thaddeus P Dryja

Nature genetics, Vol.1(3), pp.209-213

1992-06

PMID: 1303237

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Citation topics: 1 Clinical & Life Sciences; 1.36 Ophthalmology; 1.36.212 Retina
Web Of Science research areas: Genetics & Heredity
ESI research areas: Molecular Biology & Genetics

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Title: A Null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosa
Creators: Philip J Rosenfeld
Glenn S Cowley
Terri L McGee
Michael A Sandberg
Eliot L Berson
Thaddeus P Dryja
Publication Details: Nature genetics, Vol.1(3), pp.209-213
Academic Unit: Miller School of Medicine; UMMG Department of Ophthalmology
Language: English
Resource Type: Journal article
PMID: 1303237
Record Identifier: 991031600237302976