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Mutations in SCG10 Are Not Involved in Hirschsprung Disease
Hirschsprung disease (HSCR) is a congenital malformation characterized by the absence of enteric neurons in the distal part of the colon. Several genes have been implicated in the development of this disease that together account for 20% of all cases, implying that other genes are involved. Since HS...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3004862/ https://ncbi.nlm.nih.gov/pubmed/21187955 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0015144 |
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