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Whole Exome Sequencing Identifies Multiple, Complex Etiologies in an Idiopathic Hereditary Pancreatitis Kindred

CONTEXT: Hereditary pancreatitis is the early onset form of chronic pancreatitis that is carried in an autosomal dominant pattern with variable penetrance. While 80% of HP has been shown to be due to a single mutation in the trypsinogen gene PRSS1, a number of HP families have no identified genetic...

詳細記述

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書誌詳細
主要な著者: LaRusch, Jessica, Barmada, M. Michael, Solomon, Sheila, Whitcomb, David C.
フォーマット: Artigo
言語:Inglês
出版事項: 2012
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC3651649/
https://ncbi.nlm.nih.gov/pubmed/22572128
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