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Missense mutations in EYA1 and TCF2 are a rare cause of urinary tract malformations
- Source :
- Nephrology Dialysis Transplantation. 23:777-779
- Publication Year :
- 2007
- Publisher :
- Oxford University Press (OUP), 2007.
- Subjects :
- Adult
Male
Adolescent
Urinary system
Mutation, Missense
Protein tyrosine phosphatase
Humans
Medicine
Missense mutation
Nuclear protein
Child
Urinary Tract
Aged
Hepatocyte Nuclear Factor 1-beta
Transplantation
business.industry
Intracellular Signaling Peptides and Proteins
Nuclear Proteins
Middle Aged
Nephrology
Child, Preschool
Hepatocyte Nuclear Factor 1-Beta
Cancer research
Female
Protein Tyrosine Phosphatases
business
Subjects
Details
- ISSN :
- 14602385 and 09310509
- Volume :
- 23
- Database :
- OpenAIRE
- Journal :
- Nephrology Dialysis Transplantation
- Accession number :
- edsair.doi.dedup.....6dfb7f7b7f70856d59eeb5c3f6d6c9e6