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Q39141569-FAC724C8-6C2D-4B6A-942D-E32C939B4213
Q39141569-FAC724C8-6C2D-4B6A-942D-E32C939B4213
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Statement
http://www.wikidata.org/entity/statement/Q39141569-FAC724C8-6C2D-4B6A-942D-E32C939B4213
Renal aplasia in humans is associated with RET mutations.
P2860
Q39141569-FAC724C8-6C2D-4B6A-942D-E32C939B4213
BestRank
Statement
http://www.wikidata.org/entity/statement/Q39141569-FAC724C8-6C2D-4B6A-942D-E32C939B4213
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wasDerivedFrom
534d9ce0f7d92e6899f4528df7af5d001506a5e2
P2860
A human model for multigenic inheritance: phenotypic expression in Hirschsprung disease requires both the RET gene and a new 9q31 locus.