Interstitial 2q24.3 deletion including SCN2A and SCN3A genes in a patient with autistic features, psychomotor delay, microcephaly and no history of seizures-Reference-Cited by-同舟云学术

Interstitial 2q24.3 deletion including SCN2A and SCN3A genes in a patient with autistic features, psychomotor delay, microcephaly and no history of seizures

Published:2013-12 Issue:2 Volume:532 Page:294-296
ISSN:0378-1119
Container-title:Gene
language:en
Short-container-title:Gene

Author:

Celle Maria Elena,Cuoco Cristina,Porta Simona,Gimelli Giorgio,Tassano Elisa

Funder

Cinque per mille dell'IRPEF-Finanziamento della ricerca sanitaria

Finanziamento Ricarca Corrente, Ministero Salute

Publisher

Elsevier BV

Subject

Genetics,General Medicine

Reference15 articles.

1. Disruption of the SCN2A and SCN3A genes in a patient with mental retardation, neurobehavioral and psychiatric abnormalities, and a history of infantile seizures;Bartnik;Clin. Genet.,2011

2. Array-CGH detection of a de novo 2.8Mb deletion in 2q24.2→q24.3 in a girl with autistic features and developmental delay;Chen;Eur. J. Med. Genet.,2010

3. Deletion of the SCN gene cluster on 2q24.4 is associated with severe epilepsy: an array-based genotype–phenotype correlation and a comprehensive review of previously published cases;Davidsson;Epilepsy Res.,2008

4. Inherited disorders of voltage-gated sodium channels;George;J. Clin. Invest.,2005

5. Mutation of sodium channel SCN3A in a patient with cryptogenic pediatric partial epilepsy;Holland;Neurosci. Lett.,2008

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