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Q47273807-1B05CBFC-1DC1-4F01-9956-489920CBC8F9
Q47273807-1B05CBFC-1DC1-4F01-9956-489920CBC8F9
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http://www.wikidata.org/entity/statement/Q47273807-1B05CBFC-1DC1-4F01-9956-489920CBC8F9
Pathogenicity of a Human Laminin β2 Mutation Revealed in Models of Alport Syndrome.
P2860
Q47273807-1B05CBFC-1DC1-4F01-9956-489920CBC8F9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47273807-1B05CBFC-1DC1-4F01-9956-489920CBC8F9
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wasDerivedFrom
5109bda32595de2b6e7d9a8619a026357ba642b3
P2860
Clinico-pathological correlations in 127 patients in 11 large pedigrees, segregating one of three heterozygous mutations in the COL4A3/ COL4A4 genes associated with familial haematuria and significant late progression to proteinuria and chronic kidn