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Genetics of Prader-Willi syndrome and Prader-Will-Like syndrome

The Prader-Willi syndrome (PWS) is a human imprinting disorder resulting from genomic alterations that inactivate imprinted, paternally expressed genes in human chromosome region 15q11-q13. This genetic condition appears to be a contiguous gene syndrome caused by the loss of at least 2 of a number o...

詳細記述

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書誌詳細
出版年:Ann Pediatr Endocrinol Metab
第一著者: Cheon, Chong Kun
フォーマット: Artigo
言語:Inglês
出版事項: The Korean Society of Pediatric Endocrinology 2016
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC5073158/
https://ncbi.nlm.nih.gov/pubmed/27777904
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.6065/apem.2016.21.3.126
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