☆ 4.5 Article

Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome -: art. no. e15

JOURNAL OF MEDICAL GENETICS (2005)

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Journal

JOURNAL OF MEDICAL GENETICS
Volume 42, Issue 2, Pages -

Publisher

BMJ PUBLISHING GROUP
DOI: 10.1136/jmg.2004.026161

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Categories

Genetics & Heredity

Funding

  1. NICHD NIH HHS [HD24064, P01-HD40301, HD 38985] Funding Source: Medline

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