An electrophysiological study on children and young adults with Alport's syndrome.-Reference-Cited by-同舟云学术

An electrophysiological study on children and young adults with Alport's syndrome.

Published:1994-01-01 Issue:1 Volume:78 Page:44-48
ISSN:0007-1161
Container-title:British Journal of Ophthalmology
language:en
Short-container-title:British Journal of Ophthalmology

Author:

Jeffrey B G,Jacobs M,Sa G,Barratt T M,Taylor D,Kriss A

Publisher

BMJ

Subject

Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology

Reference36 articles.

1. Genetics of classic Alport's syndrome;Flinter, F.A.; Cameron, J.S.; Chantler, C.; Houston, I.; Bobrow, M.;Lancet,1988

2. Mapping of Alport syndrome to the long arm of the X chromosome;Atkin, C.L.; Hasstedt, S.J.; Menlove, L.; Cannon, L.; Kirschner, N.; Schwartz, C.;Am Jf Hun Genet,1988

3. Identification ofmutations in the COL4A5 collagen gene in Alport syndrome;Barker, D.F.; Hostikka, S.L.; Zhou, J.; Chow, L.T.; Oliphant, A.R.; Gerken, S.C.;Science,1990

4. Fundus changes in the hereditary nephropathies;Peterson, W.S.; Albert, D.M.;TransAmAcadOphthalmolOtolaryngol,1974

5. Macular lesions in Alport's disease;Polak, B.C.P.; Hogewind, B.L.;AmJ Ophthalmol,1977

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