Nephronophthisis related to homozygous NPHP1 gene deletion as a cause of chronic renal failure in adults
Details
Serval ID
serval:BIB_1D81F5170C5F
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Nephronophthisis related to homozygous NPHP1 gene deletion as a cause of chronic renal failure in adults
Journal
Nephrol Dial Transplant
ISSN
0931-0509 (Print)
ISSN-L
0931-0509
Publication state
Published
Issued date
09/2006
Volume
21
Number
9
Pages
2660-3
Language
english
Notes
Bollee, Guillaume
Fakhouri, Fadi
Karras, Alexandre
Noel, Laure-Helene
Salomon, Remi
Servais, Aude
Lesavre, Philippe
Moriniere, Vincent
Antignac, Corinne
Hummel, Aurelie
eng
Case Reports
England
Nephrol Dial Transplant. 2006 Sep;21(9):2660-3. doi: 10.1093/ndt/gfl348. Epub 2006 Jun 17.
Fakhouri, Fadi
Karras, Alexandre
Noel, Laure-Helene
Salomon, Remi
Servais, Aude
Lesavre, Philippe
Moriniere, Vincent
Antignac, Corinne
Hummel, Aurelie
eng
Case Reports
England
Nephrol Dial Transplant. 2006 Sep;21(9):2660-3. doi: 10.1093/ndt/gfl348. Epub 2006 Jun 17.
Keywords
Adaptor Proteins, Signal Transducing, Adult, Cytoskeletal Proteins, DNA/*genetics, Female, Follow-Up Studies, *Gene Deletion, Homozygote, Humans, Kidney Diseases, Cystic/complications/*genetics/metabolism, Kidney Failure, Chronic/*etiology/genetics/metabolism, Male, Membrane Proteins, Polymerase Chain Reaction, Proteins/*genetics
Pubmed
Create date
01/03/2022 10:18
Last modification date
02/03/2022 6:35