Identification of a New Locus for Medullary Cystic Disease, on Chromosome 16p12
- 1 June 1999
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 64 (6), 1655-1660
- https://doi.org/10.1086/302414
Abstract
No abstract availableKeywords
This publication has 31 references indexed in Scilit:
- A novel gene encoding an SH3 domain protein is mutated in nephronophthisis type 1Nature Genetics, 1997
- Concise clinical report. Late occurrence of cysts in autosomal dominant medullary cystic kidney diseaseNephrology Dialysis Transplantation, 1997
- A comprehensive genetic map of the human genome based on 5,264 microsatellitesNature, 1996
- Cloning, Chromosomal Localization, and Physical Linkage of the β and γ Subunits (SCNN1B and SCNN1G) of the Human Epithelial Amiloride-Sensitive Sodium ChannelGenomics, 1995
- Liddle's syndrome: Heritable human hypertension caused by mutations in the β subunit of the epithelial sodium channelCell, 1994
- The 1993–94 Généthon human genetic linkage mapNature Genetics, 1994
- Localization of the Tamm‐Horsfall glycoprotein (unomodulin) gene to chromosome 16p12.3‐16p13.11Annals of Human Genetics, 1993
- Overexpression of a Transporter Gene in a Multidrug-Resistant Human Lung Cancer Cell LineScience, 1992
- Identification of Human Uromodulin as the Tamm-Horsfall Urinary GlycoproteinScience, 1987
- Morphology of the ascending thick limb of HenleKidney International, 1976