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Effects ofMECP2 mutation type, location and X-inactivation in modulating Rett syndrome phenotype

✍ Scribed by Weaving, Linda S. ;Williamson, Sarah L. ;Bennetts, Bruce ;Davis, Mark ;Ellaway, Carolyn J. ;Leonard, Helen ;Thong, Meow-Keong ;Delatycki, Martin ;Thompson, Elizabeth M. ;Laing, Nigel ;Christodoulou, John


Publisher
John Wiley and Sons
Year
2003
Tongue
English
Weight
202 KB
Volume
118A
Category
Article
ISSN
0148-7299

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