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A CRX mutation in a Finnish family with dominant cone‐rod retinal dystrophy
Author(s) -
Sankila EevaMarja,
Joensuu Tarja H.,
Hämäläinen Riikka H.,
Raitanen Nina,
Valle Olavi,
Ignatius Jaakko,
Cormand Bru
Publication year - 2000
Publication title -
human mutation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.981
H-Index - 162
eISSN - 1098-1004
pISSN - 1059-7794
DOI - 10.1002/1098-1004(200007)16:1<94::aid-humu25>3.0.co;2-t
Subject(s) - medical genetics , molecular genetics , genetics , medicine , biology , gene