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RET Variants and Haplotype Analysis in a Cohort of Czech Patients with Hirschsprung Disease
Hirschsprung disease (HSCR) is a congenital aganglionosis of myenteric and submucosal plexuses in variable length of the intestine. This study investigated the influence and a possible modifying function of RET proto-oncogene's single nucleotide polymorphisms (SNPs) and haplotypes in the develo...
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| Hlavní autoři: | , , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Public Library of Science
2014
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4045806/ https://ncbi.nlm.nih.gov/pubmed/24897126 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0098957 |
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