DOI:
10.1055/s-00029030
Journal of Pediatric Neurology
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References
Nectoux J, Heron D, Tallot M, Chelly J, Bienvenu T.
Maternal origin of a novel C-terminal truncation mutation in CDKL5 causing a severe atypical form of Rett syndrome.
Clin Genet 2006;
70 (01) 29-33
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