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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Detalles Bibliográficos
Autores principales: Alves, Maria M. M., Osinga, Jan, Verheij, Joke B. G. M., Metzger, Marco, Eggen, Bart J. L., Hofstra, Robert M. W.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3004862/
https://www.ncbi.nlm.nih.gov/pubmed/21187955
http://dx.doi.org/10.1371/journal.pone.0015144

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3004862/
https://www.ncbi.nlm.nih.gov/pubmed/21187955
http://dx.doi.org/10.1371/journal.pone.0015144

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