A Rare Haplotype of the RET Proto-Oncogene Is a Risk-Modifying Allele in Hirschsprung Disease

Hirschsprung disease (HSCR) is a common genetic disorder characterized by intestinal obstruction secondary to enteric aganglionosis. HSCR demonstrates a complex pattern of inheritance, with the RET proto-oncogene acting as a major gene and with several additional susceptibility loci related to the R...

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Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Am J Hum Genet
Egile Nagusiak: Griseri, Paola, Pesce, Barbara, Patrone, Giovanna, Osinga, Jan, Puppo, Francesca, Sancandi, Monica, Hofstra, Robert, Romeo, Giovanni, Ravazzolo, Roberto, Devoto, Marcella, Ceccherini, Isabella
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Elsevier 2002
Gaiak:
Report
Sarrera elektronikoa:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC378552/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/12214285/
https://ncbi.nlm.nih.govhttps://doi.org/10.1086/342774
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