论文信息 - Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome - 字舞流文

Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome

H. Zoghbi | R. Amir | D. Glaze | A. Percy | P. Fang | B. Roa | I. B. Van den Veyver | Z. Yu | Alan K. Percy | Ping Fang | Benjamin B. Roa | I. B. V. D. Veyver