Add to ORKGSingle base pair deletions in exons 39 and 42 of the COL4A5 gene in Alport syndrom
The COL4A5 gene encodes the alpha5 (type IV) collagen chain and is defective in X-linked Alport synd...
The COL4A5 gene encodes the alpha5 (type IV) collagen chain and is defective in X-linked Alport synd...
Alport syndrome (AS) can be caused by mutations in COL4A5, one of the six type IV collagen genes. Fo...
Deletions of the COL4A5 gene in patients with Alport syndrome. Mutations in the COL4A5 gene encoding...
Mutations in the COL4A5 gene in Alport syndrome: A possible mutation in primordial germ cells. Using...
We have identified a novel missense transition (362G-->A) in exon 3 of the COL4A5 gene in a male pat...
<p>A. Exon 25 sequencing from a normal male individual. B. Sequencing from a heterozygous female. C....
The COL4A5 gene in Japanese Alport syndrome patients: Spectrum of mutations of all exons. To determi...
Alport's syndrome is characterized clinically by a nonimmune glomerulopathy, often accompanied by se...
Mutations in the codon for a conserved arginine-1563 in the COL4A5 collagen gene in Alport syndrome....
Alport syndrome (AS), a hereditary type IV collagen nephropathy, is a major cause of end-stage renal...
The gene coding for the α5 chain of type IV collagen (α5(IV) collagen), which maps to Xq22, is a can...
Small frameshift deletions within the COL4A5 gene were identified in three Alport syndrome Italian f...
Identification of a single base insertion in the COL4A5 gene in Alport syndrome. We identified a nov...
Abstract Background Alport syndrome (AS), which is a rare hereditary disease caused by mutations of ...
The COL4A5 gene encodes the alpha5 (type IV) collagen chain and is defective in X-linked Alport synd...
The COL4A5 gene encodes the alpha5 (type IV) collagen chain and is defective in X-linked Alport synd...
Alport syndrome (AS) can be caused by mutations in COL4A5, one of the six type IV collagen genes. Fo...
Deletions of the COL4A5 gene in patients with Alport syndrome. Mutations in the COL4A5 gene encoding...
Mutations in the COL4A5 gene in Alport syndrome: A possible mutation in primordial germ cells. Using...
We have identified a novel missense transition (362G-->A) in exon 3 of the COL4A5 gene in a male pat...
<p>A. Exon 25 sequencing from a normal male individual. B. Sequencing from a heterozygous female. C....
The COL4A5 gene in Japanese Alport syndrome patients: Spectrum of mutations of all exons. To determi...
Alport's syndrome is characterized clinically by a nonimmune glomerulopathy, often accompanied by se...
Mutations in the codon for a conserved arginine-1563 in the COL4A5 collagen gene in Alport syndrome....
Alport syndrome (AS), a hereditary type IV collagen nephropathy, is a major cause of end-stage renal...
The gene coding for the α5 chain of type IV collagen (α5(IV) collagen), which maps to Xq22, is a can...
Small frameshift deletions within the COL4A5 gene were identified in three Alport syndrome Italian f...
Identification of a single base insertion in the COL4A5 gene in Alport syndrome. We identified a nov...
Abstract Background Alport syndrome (AS), which is a rare hereditary disease caused by mutations of ...
The COL4A5 gene encodes the alpha5 (type IV) collagen chain and is defective in X-linked Alport synd...
The COL4A5 gene encodes the alpha5 (type IV) collagen chain and is defective in X-linked Alport synd...
Alport syndrome (AS) can be caused by mutations in COL4A5, one of the six type IV collagen genes. Fo...