Mutation in the SLC9A6 gene is not a frequent cause of sporadic Angelman-like syndrome
- PMID: 19471312
- PMCID: PMC2986687
- DOI: 10.1038/ejhg.2009.82
Mutation in the SLC9A6 gene is not a frequent cause of sporadic Angelman-like syndrome
References
-
- Williams CA, Beaudet AL, Clayton-Smith J, et al. Angelman syndrome 2005: updated consensus for diagnostic criteria. Am J Med Genet A. 2006;140:413–418. - PubMed
-
- Petersen MB, Brondum-Nielsen K, Hansen LK, Wulff K. Clinical, cytogenetic, and molecular diagnosis of Angelman syndrome: estimated prevalence rate in a Danish county. Am J Med Genet. 1995;60:261–262. - PubMed
-
- Stromme P, Hagberg G. Aetiology in severe and mild mental retardation: a population-based study of Norwegian children. Dev Med Child Neurol. 2000;42:76–86. - PubMed
-
- Thomson AK, Glasson EJ, Bittles AH. A long-term population-based clinical and morbidity profile of Angelman syndrome in Western Australia: 1953–2003. Disabil Rehabil. 2006;28:299–305. - PubMed
-
- Hou JW, Wang TR, Chuang SM. An epidemiological and aetiological study of children with intellectual disability in Taiwan. J Intellect Disabil Res. 1998;42:137–143. - PubMed
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