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Heterozygous FA2H mutations in autism spectrum disorders

✍ Scribed by Scheid, Isabelle; Maruani, Anna; Huguet, Guillaume; Leblond, Claire S; Nygren, Gudrun; Anckarsäter, Henrik; Beggiato, Anita; Rastam, Maria; Amsellem, Fréderique; Gillberg, I; Elmaleh, Monique; Leboyer, Marion; Gillberg, Christopher; Betancur, Catalina; Coleman, Mary; Hama, Hiroko; Cook, Edwin H; Bourgeron, Thomas; Delorme, Richard

Book ID
121588789
Publisher
BioMed Central
Year
2013
Tongue
English
Weight
812 KB
Volume
14
Category
Article
ISSN
1471-2350

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## Abstract Linkage to 7q has been the most robust genetic finding in familial autism. A previous scan of multiplex families with autism spectrum disorders found a linkage signal of genome‐wide significance at D7S530 on 7q32. We searched a candidate imprinted region at this location for genetic var