Differential Gene Expression Reveals Mitochondrial Dysfunction in an Imprinting Center Deletion Mouse Model of Prader–Willi Syndrome

Prader–Willi syndrome (PWS) is a genetic disorder caused by deficiency of imprinted gene expression from the paternal chromosome 15q11–15q13 and clinically characterized by neonatal hypotonia, short stature, cognitive impairment, hypogonadism, hyperphagia, morbid obesity, and diabetes. Previous clin...

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Main Authors: Yazdi, Puya G., Su, Hailing, Ghimbovschi, Svetlana, Fan, Weiwei, Coskun, Pinar E., Nalbandian, Angèle, Knoblach, Susan, Resnick, James L., Hoffman, Eric, Wallace, Douglas C., Kimonis, Virginia E.
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2013
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Research Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3815468/
https://ncbi.nlm.nih.gov/pubmed/24127921
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/cts.12083
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