User: Guest  Login
Title:

The 2019 and 2021 International Workshops on Alport Syndrome.

Document type:
Journal Article; Research Support, Non-U.S. Gov't; Research Support, N.I.H., Extramural
Author(s):
Daga, Sergio; Ding, Jie; Deltas, Constantinos; Savige, Judy; Lipska-Ziętkiewicz, Beata S; Hoefele, Julia; Flinter, Frances; Gale, Daniel P; Aksenova, Marina; Kai, Hirofumi; Perin, Laura; Barua, Moumita; Torra, Roser; Miner, Jeff H; Massella, Laura; Ljubanović, Danica Galešić; Lennon, Rachel; Weinstock, Andrè B; Knebelmann, Bertrand; Cerkauskaite, Agne; Gear, Susie; Gross, Oliver; Turner, A Neil; Baldassarri, Margherita; Pinto, Anna Maria; Renieri, Alessandra
Abstract:
In 1927 Arthur Cecil Alport, a South African physician, described a British family with an inherited form of kidney disease that affected males more severely than females and was sometimes associated with hearing loss. In 1961, the eponymous name Alport syndrome was adopted. In the late twentieth century three genes responsible for the disease were discovered: COL4A3, COL4A4, and COL4A5 encoding for the α3, α4, α5 polypeptide chains of type IV collagen, respectively. These chains assemble to for...     »
Journal title abbreviation:
Eur J Hum Genet
Year:
2022
Journal volume:
30
Journal issue:
5
Pages contribution:
507-516
Fulltext / DOI:
doi:10.1038/s41431-022-01075-0
Pubmed ID:
http://view.ncbi.nlm.nih.gov/pubmed/35260866
Print-ISSN:
1018-4813
TUM Institution:
Institut für Humangenetik
 BibTeX