Molecular Investigation of Distal Renal Tubular Acidosis in Tunisia, Evidence for Founder Mutations

Background: Distal renal tubular acidosis (dRTA) is a rare genetic disease caused by mutations in different genes involved in the secretion of H+ ions in the intercalated cells of the collecting duct. Both autosomal dominant and recessive forms have been described; the latter is also associated with...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Asıl Yazarlar: Nagara, Majdi, Voskarides, Konstantinos, Nouira, Sonia, Ben Halim, Nizar, Kefi, Rym, Aloulou, Hajer, Romdhane, Lilia, Ben Abdallah, Rim, Ben Rhouma, Faten, Aissa, Khaoula, Boughamoura, Lamia, Kammoun, Thouraya, Azzouz, Hatem, Abroug, Saoussen, Ben Turkia, Hathemi, Ayadi, Abdelkarim, Mrad, Ridha, Chabchoub, Imen, Hachicha, Mongia, Chemli, Jalel, Deltas, Constantinos, Abdelhak, Sonia
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Mary Ann Liebert, Inc. 2014
Konular:
Original Articles
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4217022/
https://ncbi.nlm.nih.gov/pubmed/25285676
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/gtmb.2014.0175
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!

Benzer Materyaller