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MECP2 mutations account for most cases of typical forms of Rett syndrome

✍ Scribed by Bienvenu, T.

Book ID: 121711013
Publisher: Oxford University Press
Year: 2000
Tongue: English
Weight: 661 KB
Volume: 9
Category: Article
ISSN: 0964-6906
DOI: 10.1093/hmg/9.9.1377

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