Clinical characterization, linkage analysis, and PRPC8 mutation analysis of a family with autosomal dominant retinitis pigmentosa type 13 (RP13)

Author: van Lith-Verhoeven J.J.C.   van der Velde-Visser S.D.   Sohocki M.M.   Deutman A.F.   Brink H.M.A.   Cremers F.P.M.   Hoyng C.B.  

Publisher: Informa Healthcare

ISSN: 1381-6810

Source: Ophthalmic Genetics, Vol.23, Iss.1, 2002-03, pp. : 1-12

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content