DOI:
10.1055/s-00029030
Journal of Pediatric Neurology
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References
Hadzsiev K, Polgar N, Bene J. et al.
Analysis of Hungarian patients with Rett syndrome phenotype for MECP2, CDKL5 and FOXG1 gene mutations.
J Hum Genet 2011;
56 (03) 183-187
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