𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Multiplex Targeted Sequencing Identifies Recurrently Mutated Genes in Autism Spectrum Disorders

✍ Scribed by O'Roak, Brian J. (author);Vives, Laura (author);Fu, Wenqing (author);Egertson, Jarrett D. (author);Stanaway, Ian B. (author);Phelps, Ian G. (author);Carvill, Gemma (author);Kumar, Akash (author);Lee, Choli (author);Ankenman, Katy (author);Munson, Jeff (author);Hiatt, Joseph B. (author);Turner, Emily H. (author);Levy, Roie (author);O'Day, Diana R. (author);Krumm, Niklas (author);Coe, Bradley P. (author);Martin, Beth K. (author);Borenstein, Elhanan (author);Nickerson, Deborah A. (author);Mefford, Heather C. (author);Doherty, Dan (author);Akey, Joshua M. (author);Bernier, Raphael (author);Eichler, Evan E. (author);Shendure, Jay (author)

Book ID
118015427
Publisher
American Association for the Advancement of Science
Year
2012
Tongue
English
Weight
645 KB
Volume
338
Category
Article
ISSN
0036-8075

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Mutations in the TSGA14 gene in families
Mutations in the TSGA14 gene in families with autism spectrum disorders
✍ O. Korvatska; A. Estes; J. Munson; G. Dawson; L.M. Bekris; R. Kohen; C.-E. Yu; G πŸ“‚ Article πŸ“… 2011 πŸ› John Wiley and Sons 🌐 English βš– 299 KB πŸ‘ 2 views

## 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