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Q55339157-F6FEEB3B-4980-49A5-957A-88A5E7656B89
Q55339157-F6FEEB3B-4980-49A5-957A-88A5E7656B89
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Statement
http://www.wikidata.org/entity/statement/Q55339157-F6FEEB3B-4980-49A5-957A-88A5E7656B89
Identification of a novel UMOD mutation (c.163G>A) in a Brazilian family with autosomal dominant tubulointerstitial kidney disease.
P2860
Q55339157-F6FEEB3B-4980-49A5-957A-88A5E7656B89
BestRank
Statement
http://www.wikidata.org/entity/statement/Q55339157-F6FEEB3B-4980-49A5-957A-88A5E7656B89
rank
NormalRank
type
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Statement
wasDerivedFrom
ef032b69d999c08dc824c551818f9602f9ff0d46
P2860
Heterozygous Loss-of-Function SEC61A1 Mutations Cause Autosomal-Dominant Tubulo-Interstitial and Glomerulocystic Kidney Disease with Anemia