Parental origin of de novo MECP2 mutations in Rett syndrome.
Girard M; Couvert P; Carrié A; Tardieu M; Chelly J; Beldjord C; Bienvenu T; European Journal Of Human Genetics: EJHG, 2001, vol. 9, issue 3, p 231, ISSN 10184813. ISBN 10184813.

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