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Q42685074-824BFB47-E482-48E9-A1F3-77CE66E3CBB3
Q42685074-824BFB47-E482-48E9-A1F3-77CE66E3CBB3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42685074-824BFB47-E482-48E9-A1F3-77CE66E3CBB3
Hypomorphic mutation in TTC7A causes combined immunodeficiency with mild structural intestinal defects
P2860
Q42685074-824BFB47-E482-48E9-A1F3-77CE66E3CBB3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42685074-824BFB47-E482-48E9-A1F3-77CE66E3CBB3
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wasDerivedFrom
b6d33172734ac6f7fe4be167e5ad71250cd0c469
P2860
Whole-exome sequencing identifies tetratricopeptide repeat domain 7A (TTC7A) mutations for combined immunodeficiency with intestinal atresias.