ATRX has a critical and conserved role in mammalian sexual differentiation

BACKGROUND: X-linked alpha thalassemia, mental retardation syndrome in humans is a rare recessive disorder caused by mutations in the ATRX gene. The disease is characterised by severe mental retardation, mild alpha-thalassemia, microcephaly, short stature, facial, skeletal, genital and gonadal abnor...

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Detalles Bibliográficos
Autores principales: Huyhn, Kim, Renfree, Marilyn B, Graves, Jennifer A, Pask, Andrew J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3133603/
https://www.ncbi.nlm.nih.gov/pubmed/21672208
http://dx.doi.org/10.1186/1471-213X-11-39

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3133603/
https://www.ncbi.nlm.nih.gov/pubmed/21672208
http://dx.doi.org/10.1186/1471-213X-11-39

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