Polycystic kidney disease: DZIP1L defines a new functional zip code for autosomal recessive PKD

Nat Rev Nephrol. 2017 Sep;13(9):519-520. doi: 10.1038/nrneph.2017.102. Epub 2017 Jul 24.

Authors

Erum A Hartung¹, Lisa M Guay-Woodford²

Affiliations

¹ Division of Nephrology, Children's Hospital of Philadelphia; Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, 3401 Civic Center Boulevard; Philadelphia, Pennsylvania 19104, USA.
² Center for Translational Science, Children's National Health System, 6 th Floor Main Hospital, Center 6, 111 Michigan Ave NW, Washington, District of Columbia 20010, USA.

PMID: 28736432
DOI: 10.1038/nrneph.2017.102

No abstract available

Publication types

News

MeSH terms

Adaptor Proteins, Signal Transducing / genetics*
Cilia / genetics
Cilia / pathology*
Genetic Markers
Humans
Phenotype
Polycystic Kidney, Autosomal Recessive / genetics*
Polycystic Kidney, Autosomal Recessive / pathology

Substances

Adaptor Proteins, Signal Transducing
DZIP1L protein, human
Genetic Markers

Grants and funding

K23 DK109203/DK/NIDDK NIH HHS/United States