Investigation of the 15q13.3 CNV as a genetic modifier for familial epilepsies with variable phenotypes
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Investigation of 15q11-q13, 16p11.2 and 22q13 CNVs in autism spectrum disorder Brazilian individuals with and without epilepsy.Where genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited disease.Association study of the 2-bp deletion polymorphism in exon 6 of the CHRFAM7A gene with idiopathic generalized epilepsy.The role of T-type calcium channel genes in absence seizures.Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy.
P2860
Investigation of the 15q13.3 CNV as a genetic modifier for familial epilepsies with variable phenotypes
description
article
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im Juli 2011 veröffentlichter wissenschaftlicher Artikel
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wetenschappelijk artikel
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наукова стаття, опублікована в липні 2011
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name
Investigation of the 15q13.3 C ...... psies with variable phenotypes
@en
Investigation of the 15q13.3 C ...... psies with variable phenotypes
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type
label
Investigation of the 15q13.3 C ...... psies with variable phenotypes
@en
Investigation of the 15q13.3 C ...... psies with variable phenotypes
@nl
prefLabel
Investigation of the 15q13.3 C ...... psies with variable phenotypes
@en
Investigation of the 15q13.3 C ...... psies with variable phenotypes
@nl
P2093
P2860
P50
P1433
P1476
Investigation of the 15q13.3 C ...... psies with variable phenotypes
@en
P2093
Bronwyn E Grinton
Danya F Vears
John C Mulley
Marta A Bayly
Tarishi Desai
P2860
P304
P356
10.1111/J.1528-1167.2011.03188.X
P577
2011-07-21T00:00:00Z