Autosomal recessive Alport’s syndrome and benign familial hematuria are collagen type IV diseases

Author:

Vega Bárbara Tazón,Badenas Cèlia,Ars Elisabet,Lens Xose,Milà Montse,Darnell Alejandro,Torra Roser

Publisher

Elsevier BV

Subject

Nephrology

Reference36 articles.

1. The genes coding for human pro alpha 1(IV) collagen and pro alpha 2(IV) collagen are both located at the end of the long arm of chromosome 13;Boyd;Am J Hum Genet,1988

2. Colocalization of the genes for the alpha 3(IV) and alpha 4(IV) chains of type IV collagen to chromosome 2 bands q35-q37;Mariyama;Genomics,1992

3. Molecular cloning of alpha 5(IV) collagen and assignment of the gene to the region of the X chromosome containing the Alport syndrome locus;Myers;Am J Hum Genet,1990

4. Identification of a new collagen IV chain, alpha 6(IV), by cDNA isolation and assignment of the gene to chromosome Xq22, which is the same locus for COL4A5;Oohashi;J Biol Chem,1994

5. Hereditary familial congenital haemorrhagic nephritis;Alport;Br Med J,1927

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