Work

Autosomal dominant hypocalcaemia caused by a Ca2+-sensing receptor gene mutation

Year: 1994

Type: article

Source: Nature Genetics

DOI: 10.1038/ng1194-303

Authors: Martin R. Pollak, Edward M. Brown, Herschel L. Estep, Peter N. McLaine, Olga Kifor, Ji Park, Steven C. Hebert, Christine E. Seidman, J. G. Seidman

Institutions: Brigham and Women's Hospital, Eastern Virginia Medical School, Children's Hospital of Eastern Ontario, Howard Hughes Medical Institute, Harvard University

Language: English

Topic: Parathyroid Disorders and Treatments

Subfield: Nephrology

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases

Awards: G2941642409, G35286316, GENETICS OF FAMILIAL HYPOCALCIURIC HYPERCALCEMIA, PHOSPHOLIPASES AND CA++/REGULATED PARATHYROID FUNCTION, HOMOLOGOUS RECOMBINATION TO INACTIVATE MOUSE ANP, G674121311

OpenAlex ID: W2010599278

FWCI: 26.32

Cites: 21

Cited by: 592

Related to: 10