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Frequent Loss of Genome Gap Region in 4p16.3 Subtelomere in Early-Onset Type 2 Diabetes Mellitus

A small portion of Type 2 diabetes mellitus (T2DM) is familial, but the majority occurs as sporadic disease. Although causative genes are found in some rare forms, the genetic basis for sporadic T2DM is largely unknown. We searched for a copy number abnormality in 100 early-onset Japanese T2DM patie...

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Detalhes bibliográficos
Main Authors: Kudo, Hirohito, Emi, Mitsuru, Ishigaki, Yasushi, Tsunoda, Uiko, Hinokio, Yoshinori, Ishii, Miho, Sato, Hidenori, Yamada, Tetsuya, Katagiri, Hideki, Oka, Yoshitomo
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi Publishing Corporation 2011
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3132460/
https://ncbi.nlm.nih.gov/pubmed/21754918
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2011/498460
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