A necdin/MAGE-like gene in the chromosome 15 autism susceptibility region: expression, imprinting, and mapping of the human and mouse orthologues

BACKGROUND: Proximal chromosome 15q is implicated in neurodevelopmental disorders including Prader-Willi and Angelman syndromes, autistic disorder and developmental abnormalities resulting from chromosomal deletions or duplications. A subset of genes in this region are subject to genomic imprinting,...

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Detalles Bibliográficos
Autores principales: Chibuk, Thea K, Bischof, Jocelyn M, Wevrick, Rachel
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2001
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC64493/
https://www.ncbi.nlm.nih.gov/pubmed/11782285
http://dx.doi.org/10.1186/1471-2156-2-22

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC64493/
https://www.ncbi.nlm.nih.gov/pubmed/11782285
http://dx.doi.org/10.1186/1471-2156-2-22

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