Intellectual disability associated with a homozygous missense mutation in THOC6

BACKGROUND: We recently described a novel autosomal recessive neurodevelopmental disorder with intellectual disability in four patients from two related Hutterite families. Identity-by-descent mapping localized the gene to a 5.1 Mb region at chromosome 16p13.3 containing more than 170 known or predi...

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Detalles Bibliográficos
Autores principales: Beaulieu, Chandree L, Huang, Lijia, Innes, A Micheil, Akimenko, Marie-Andree, Puffenberger, Erik G, Schwartz, Charles, Jerry, Paul, Ober, Carole, Hegele, Robert A, McLeod, D Ross, Schwartzentruber, Jeremy, Majewski, Jacek, Bulman, Dennis E, Parboosingh, Jillian S, Boycott, Kym M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3644499/
https://www.ncbi.nlm.nih.gov/pubmed/23621916
http://dx.doi.org/10.1186/1750-1172-8-62

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3644499/
https://www.ncbi.nlm.nih.gov/pubmed/23621916
http://dx.doi.org/10.1186/1750-1172-8-62

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