Phenotypic variability in two infants sharing the same MECP2 mutation: evidence of chromosomal rearrangements and high sister-chromatid exchange levels in Rett syndrome

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Authors: Marwa Kharrat, Ines Hsairi, Hajer Doukali, Nourhene Fendri-Kriaa, Hassen Kammoun, Leila Ammar-keskes, Chahnez Triki, Faiza Fakhfakh

Journal title: Acta Neurologica Belgica

Journal number: 117/1

Journal publisher: Acta Medica Belgica

Published year: 2017

Published pages: 251-258

DOI identifier: 10.1007/s13760-016-0667-5

ISSN: 0300-9009