Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

An Analysis of ABCR Mutations in British Patients with Recessive Retinal Dystrophies

Autor: Papaioannou, Myrto G., Bhattacharya, Shom Shanker

Publikováno v: Digital.CSIC. Repositorio Institucional del CSIC
instname

4 páginas, 3 tablas.-- et al.
[Purpose]: Several reports have shown that mutations in the ABCR gene can lead to Stargardt disease (STGD)/fundus flavimaculatus (FFM), autosomal recessive retinitis pigmentosa (arRP), and autosomal recessive cone-

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::ee420be9f636d4156362f27eafe76e96
http://hdl.handle.net/10261/40540

Mutations in HPRP3, a third member of pre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosa.

Autor: Chakarova CF; Department of Molecular Genetics, Institute of Ophthalmology, University College London, 11-43 Bath Street, London EC1V 9EV, UK., Hims MM, Bolz H, Abu-Safieh L, Patel RJ, Papaioannou MG, Inglehearn CF, Keen TJ, Willis C, Moore AT, Rosenberg T, Webster AR, Bird AC, Gal A, Hunt D, Vithana EN, Bhattacharya SS

Publikováno v: Human molecular genetics [Hum Mol Genet] 2002 Jan 01; Vol. 11 (1), pp. 87-92.