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
Author(s)
Bollee G., Fakhouri F., Karras A., Noel L. H., Salomon R., Servais A., Lesavre P., Moriniere V., Antignac C., Hummel A.
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.
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
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