论文信息 - Mutations in TRPM1 are a common cause of complete congenital stationary night blindness. - 字舞流文

Mutations in TRPM1 are a common cause of complete congenital stationary night blindness.

M. Kamermans | F. Riemslag | M. McCall | Mieke M. C. Bijveld | F. Meire | A. Bergen | R. Gregg | M. V. van Genderen | R. Florijn | J. Pearring | Y. Claassen