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s41431-017-0053-7
s41431-017-0053-7
https://scigraph.springernature.com/pub.10.1038/s41431-017-0053-7
Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locus.
P2888
Q48146651-F4980F80-6E4F-4998-BE2C-7DADE913DA56
P2888
s41431-017-0053-7
https://scigraph.springernature.com/pub.10.1038/s41431-017-0053-7