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Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease
Hirschsprung disease (HSCR) is the most common cause of neonatal intestinal obstruction. It is characterized by the absence of ganglia in the nerve plexuses of the lower gastrointestinal tract. So far, three common disease-susceptibility variants at the RET, SEMA3 and NRG1 loci have been detected th...
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| 出版年: | Hum Mol Genet |
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| 主要な著者: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Oxford University Press
2016
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| 主題: | |
| オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6078638/ https://ncbi.nlm.nih.gov/pubmed/27702942 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddw333 |
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