FOXP2 Is Not a Major Susceptibility Gene for Autism or Specific Language Impairment

The FOXP2 gene, located on human 7q31 (at the SPCH1 locus), encodes a transcription factor containing a polyglutamine tract and a forkhead domain. FOXP2 is mutated in a severe monogenic form of speech and language impairment, segregating within a single large pedigree, and is also disrupted by a tra...

Полное описание

Сохранить в:
Библиографические подробности
Главные авторы: Newbury, D. F., Bonora, E., Lamb, J. A., Fisher, S. E., Lai, C. S. L., Baird, G., Jannoun, L., Slonims, V., Stott, C. M., Merricks, M. J., Bolton, P. F., Bailey, A. J., Monaco, A. P.
Формат: Artigo
Язык:Inglês
Опубликовано: The American Society of Human Genetics 2002
Предметы:
Report
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC447606/
https://ncbi.nlm.nih.gov/pubmed/11894222
Метки: Добавить метку
Нет меток, Требуется 1-ая метка записи!

Схожие документы