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Protein-Truncation Mutations in the RP2 Gene in a North American Cohort of Families with X-Linked Retinitis Pigmentosa
Journal article   Open access  Peer reviewed

Protein-Truncation Mutations in the RP2 Gene in a North American Cohort of Families with X-Linked Retinitis Pigmentosa

Alan J Mears, Linn Gieser, Denise Yan, Cynthia Chen, Stacey Fahrner, Suja Hiriyanna, Ricardo Fujita, Samuel G Jacobson, Paul A Sieving and Anand Swaroop
American journal of human genetics, Vol.64(3), pp.897-900
1999
PMCID: PMC1377809
PMID: 10053026

Abstract

Retina Eye disease Photoreceptor degeneration X chromosome Genetic diagnosis
url
https://doi.org/10.1086/302298View
Published (Version of record) Open

InCites Highlights

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Collaboration types
Domestic collaboration
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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#3 Good Health and Well-Being

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