Abstract
Nonsyndromic Hirschsprung disease, hitherto assumed to be a multifactorial disease with a threshold effect due to an unknown number of genes, has been genetically dissected and shown to result from an interaction between just three loci, two of which have not previously been associated with the disease. Oligogenic inheritance can explain the main aspects of its genetic epidemiology.
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CITATION STYLE
APA
Passarge, E. (2002, May). Dissecting Hirschsprung disease. Nature Genetics. https://doi.org/10.1038/ng878
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