Rett Syndrome and Beyond: Recurrent Spontaneous and Familial MECP2 Mutations at CpG Hotspots
Wan, Mimi, Lee, Stephen Sung Jae, Zhang, Xianyu, Houwink-Manville, Isa, Song, Hae-Ri, Amir, Ruthie E., Budden, Sarojini, Naidu, SakkuBai, Pereira, Jose Luiz P., Lo, Ivan F.M., Zoghbi, Huda Y., Schanen, N. Carolyn, Francke, Uta
Published in American journal of human genetics (01.12.1999)
Published in American journal of human genetics (01.12.1999)
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