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Q40231818-35FC7BDC-AA1D-41E5-A272-4DD31BC94546
Q40231818-35FC7BDC-AA1D-41E5-A272-4DD31BC94546
BestRank
Statement
http://www.wikidata.org/entity/statement/Q40231818-35FC7BDC-AA1D-41E5-A272-4DD31BC94546
A Novel TBX19 Gene Mutation in a Case of Congenital Isolated Adrenocorticotropic Hormone Deficiency Presenting with Recurrent Respiratory Tract Infections.
P921
Q40231818-35FC7BDC-AA1D-41E5-A272-4DD31BC94546
BestRank
Statement
http://www.wikidata.org/entity/statement/Q40231818-35FC7BDC-AA1D-41E5-A272-4DD31BC94546
rank
NormalRank
type
BestRank
Statement
P921
birth defect