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Q41789233-A5FB6C57-EB74-4D59-BE36-B1D719DBCFE8
Q41789233-A5FB6C57-EB74-4D59-BE36-B1D719DBCFE8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41789233-A5FB6C57-EB74-4D59-BE36-B1D719DBCFE8
A novel LMX1B mutation in a family with end-stage renal disease of 'unknown cause'.
P2860
Q41789233-A5FB6C57-EB74-4D59-BE36-B1D719DBCFE8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41789233-A5FB6C57-EB74-4D59-BE36-B1D719DBCFE8
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wasDerivedFrom
441d75404180cef521672bf9214aaef10234b2c2
P2860
Genetic testing can resolve diagnostic confusion in Alport syndrome.