A Frameshift Mutation in Golden Retriever Dogs with Progressive Retinal Atrophy Endorses SLC4A3 as a Candidate Gene for Human Retinal Degenerations

Estimation of prognosis and prevalence of retinitis pigmentosa and Usher syndrome in Norway

(2010) J. GRøNDAHL   CLINICAL GENETICS

MTM1 mutation associated with X-linked myotubular myopathy in Labrador Retrievers

(2010) A. H. Beggs et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Prevalence of retinitis pigmentosa and allied disorders in Denmark

(2009) Marianne Haim et al.   ACTA OPHTHALMOLOGICA

Molecular physiology and genetics of Na+-independent SLC4 anion exchangers

(2009) S. L. Alper   JOURNAL OF EXPERIMENTAL BIOLOGY

Canine RD3 mutation establishes rod-cone dysplasia type 2 (rcd2) as ortholog of human and murine rd3

(2009) Anna V. Kukekova et al.   MAMMALIAN GENOME

A deletion in nephronophthisis 4 (NPHP4) is associated with recessive cone-rod dystrophy in standard wire-haired dachshund

(2008) A. C. Wiik et al.   GENOME RESEARCH

Effect of Gene Therapy on Visual Function in Leber's Congenital Amaurosis

(2008) James W.B. Bainbridge et al.   NEW ENGLAND JOURNAL OF MEDICINE