Effects of MECP2 mutation type, location and X‐inactivation in modulating Rett syndrome phenotype
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N. Laing | J. Christodoulou | H. Leonard | Mark R. Davis | M. Delatycki | C. Ellaway | M. Thong | B. Bennetts | S. Williamson | L. Weaving | Elizabeth Thompson | M. Davis | Linda S. Weaving | Elizabeth M. Thompson