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Evaluating PVALB as a candidate gene for SLC12A3-negative cases of Gitelman's syndrome
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Document type | Article de périodique (Journal article) – Article de recherche |
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Access type | Accès restreint |
Publication date | 2008 |
Language | Anglais |
Journal information | "Nephrology, Dialysis, Transplantation" - Vol. 23, no. 10, p. 3120-3125 (2008) |
Peer reviewed | yes |
Publisher | Oxford University Press ((United Kingdom) Oxford) |
issn | 0931-0509 |
e-issn | 1460-2385 |
Publication status | Publié |
Affiliations |
UCL
- MD/MINT - Département de médecine interne UCL - (SLuc) Service de néphrologie UCL - (SLuc) Centre de pathologie anorectale de l'enfant |
MESH Subject | Symporters - genetics ; Receptors, Drug - genetics ; Polymorphism, Single Nucleotide ; Parvalbumins - genetics ; Mutation ; Humans ; Gitelman Syndrome - genetics ; Genetic Variation ; Gene Frequency ; DNA Primers - genetics ; DNA Mutational Analysis ; Case-Control Studies ; Base Sequence ; Alleles |
Keywords | Distal convoluted tubule (DCT) ; NCC ; Parvalbumin ; Sodium-chloride cotransporter ; Thiazide |
Links |
Bibliographic reference | Riveira-Munoz, Eva ; Devuyst, Olivier ; Belge, Hendrica ; Jeck, Nikola ; Strompf, Laurence ; et. al. Evaluating PVALB as a candidate gene for SLC12A3-negative cases of Gitelman's syndrome. In: Nephrology, Dialysis, Transplantation, Vol. 23, no. 10, p. 3120-3125 (2008) |
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Permanent URL | http://hdl.handle.net/2078.1/12533 |