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Phenotypic variability in two infants sharing the sameMECP2mutation: evidence of chromosomal rearrangements and high sister-chromatid exchange levels in Rett syndrome
Kharrat, Marwa, Hsairi, Ines, Doukali, Hajer, Fendri-Kriaa, Nourhene, Kammoun, Hassen, Ammar-keskes, Leila, Triki, Chahnez, Fakhfakh, FaizaVolume:
117
Language:
english
Journal:
Acta Neurologica Belgica
DOI:
10.1007/s13760-016-0667-5
Date:
March, 2017
File:
PDF, 2.09 MB
english, 2017