Mutation analysis of MECP2 and determination of the X-inactivation pattern in Hungarian Rett syndrome patients.

Title:	Mutation analysis of MECP2 and determination of the X-inactivation pattern in Hungarian Rett syndrome patients.
Author(s):	Karteszi, J. Hollody, K. Bene, J. Morava, E. (298976846) Hadzsiev, K. Czako, M. Melegh, B. Teszas, A. Kosztolanyi, G.Y.
Publication year:	2004
Document type:	Article / Letter to editor
Journal:	American Journal of Medical Genetics Part A
ISSN:	1552-4825
Volume:	vol. 131
Issue:	iss. 1
Start page:	p. 106
End page:	p. 106
Subject:	UMCN 5.1: Genetic defects of metabolism
Organization:	UMCN Extern Paediatrics
Appears in Collections:	Academic bibliography

Please use this identifier to cite or link to this item: http://hdl.handle.net/2066/58651