论文信息 - A Tyr368His RPE65 founder mutation is associated with variable expression and progression of early onset retinal dystrophy in 10 families of a genetically isolated population - 字舞流文

A Tyr368His RPE65 founder mutation is associated with variable expression and progression of early onset retinal dystrophy in 10 families of a genetically isolated population

H. Brunner | F. Cremers | S. Yzer | M. Genderen | L. I. van den Born | M. V. van Genderen | R. Koenekoop | H. Kroes | L. V. D. Born | B. van den Helm | J. Schuil | F. N. Boonstra | Suzanne Yzer | H. Brunner | B. V. D. Helm | S. Yzer