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MECP2 Mutations in Sporadic Cases of Rett Syndrome Are Almost Exclusively of Paternal Origin

✍ Scribed by R. Trappe; F. Laccone; J. Cobilanschi; M. Meins; P. Huppke; F. Hanefeld; W. Engel

Book ID: 117853598
Publisher: American Society of Human Genetics
Year: 2001
Tongue: English
Weight: 182 KB
Volume: 68
Category: Article
ISSN: 0002-9297
DOI: 10.1086/320109

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