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Titel:

The 2019 and 2021 International Workshops on Alport Syndrome.

Dokumenttyp:
Journal Article; Research Support, Non-U.S. Gov't; Research Support, N.I.H., Extramural
Autor(en):
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...     »
Zeitschriftentitel:
Eur J Hum Genet
Jahr:
2022
Band / Volume:
30
Heft / Issue:
5
Seitenangaben Beitrag:
507-516
Volltext / DOI:
doi:10.1038/s41431-022-01075-0
PubMed:
http://view.ncbi.nlm.nih.gov/pubmed/35260866
Print-ISSN:
1018-4813
TUM Einrichtung:
Institut für Humangenetik
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