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Localization of the gene for X-linked Alport's syndrome

✍ Scribed by Brunner, Han; Schröder, Cock; van Bennekom, Cor; Lambermon, Eric; Tuerlings, Joep; Menzel, Daria; Olbing, Hermann; Monnens, Leo; Wieringa, Berend; Ropers, Hans-Hilger

Book ID
109881103
Publisher
Nature Publishing Group
Year
1988
Tongue
English
Weight
270 KB
Volume
34
Category
Article
ISSN
0085-2538

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Alport syndrome is a progressive renal disease leading to chronic renal failure, which often is accompanied by sensorineural deafness and ophthalmological signs in the form of anterior lenticonus. The X-linked form of the disease is caused by mutations in the COL4A5 gene encoding the a5-chain of typ