Work

Analysis of the OA1 gene reveals mutations in only one-third of patients with X-linked ocular albinism

Year: 1995

Type: article

Study design: Observational Study

Source: Human Molecular Genetics

DOI: 10.1093/hmg/4.12.2319

Authors: M.Vittoria Schiaffino, Maria T. Bassi, Lucia Galli, Alessandra Renieri, Mirella Bruttini, Filomena De Nigris, Arthur A.B. Bergen, Stephen J. Charles, John R.W. Yates, Alfons Meindl, Richard A. Lewis, Richard A. King, Andrea Ballabio

Institutions: Telethon Institute Of Genetics And Medicine, University of Siena, Manchester Royal Eye Hospital, Addenbrooke's Hospital, Ludwig-Maximilians-Universität München, Baylor College of Medicine, University of Minnesota

Language: English

Topic: Retinal Development and Disorders

Subfield: Molecular Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W2006800977

FWCI: 1.657

Cites:

Cited by: 84

Related to: 10