MECP2 Mutations and Rett Syndrome Phenotypes

MECP2 Mutations and Rett Syndrome Phenotypes

Seventy-one sporadic and 7 familial Rett syndrome (RTT) patients were screened for MECP2 mutations by direct sequencing and the pattern of X chromosome inactivation (XCI) was determined in 39 RTT patients at the Baylor College of Medicine, Houston, TX.

Bibliografski detalji
Glavni autor:	J Gordon Millichap
Format:	Članak
Jezik:	English
Izdano:	Pediatric Neurology Briefs Publishers 2000-05-01
Serija:	Pediatric Neurology Briefs
Teme:	rett syndrome milder phenotypes x chromosome inactivation
Online pristup:	https://www.pediatricneurologybriefs.com/articles/1936

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