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COL4A4 mutation in thin basement membrane disease previously described in Alport syndrome11See Editorial by Monnens, p. 799

1 Aug 2001

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 11473630
DOI: 10.1046/j.1523-1755.2001.060002480.x

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COL4A4 mutation in thin basement membrane disease previously described in Alport syndrome11See Editorial by Monnens, p. 799PMID 11473630Read ↗

COL4A3 mutations and their clinical consequences in thin basement membrane nephropathy (TBMN)Semantic proximity Read ↗

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Novel COL4A3 gene mutations in a consanguineous family with autosomal recessive Alport syndrome.Semantic proximity Read ↗

Alport syndrome: abnormalities of type IV collagen genes and proteins.Semantic proximity Read ↗

COL4A1 gene mutation--beyond a vascular syndrome.Semantic proximity Read ↗

Identification of COL4A5 defects in Alport's syndrome by immunohistochemistry of skinSemantic proximity Read ↗

Alport syndrome: a unified classification of genetic disorders of collagen IV α345: a position paper of the Alport Syndrome Classification Working Group.Semantic proximity Read ↗

Molecular genetics of basement membranes: the paradigm of Alport syndrome.Semantic proximity Read ↗

Identification of a novel COL4A5 mutation in the proband initially diagnosed as IgAN from a Chinese family with X-linked Alport syndromeSemantic proximity Read ↗

The clinical spectrum of type IV collagen mutations.Semantic proximity Read ↗

Expert consensus guidelines for the genetic diagnosis of Alport syndrome.Semantic proximity Read ↗

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