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Q36132825-39B94D11-6A01-4E2C-803D-DBCF975AB3C6
Q36132825-39B94D11-6A01-4E2C-803D-DBCF975AB3C6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36132825-39B94D11-6A01-4E2C-803D-DBCF975AB3C6
X-Linked and Autosomal Recessive Alport Syndrome: Pathogenic Variant Features and Further Genotype-Phenotype Correlations
P2860
Q36132825-39B94D11-6A01-4E2C-803D-DBCF975AB3C6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36132825-39B94D11-6A01-4E2C-803D-DBCF975AB3C6
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Statement
wasDerivedFrom
464a6f0b23c2bcef8301a39b0b4d135894f369fd
P2860
X-linked, COL4A5 hypomorphic Alport mutations such as G624D and P628L may only exhibit thin basement membrane nephropathy with microhematuria and late onset kidney failure.