Work

Mutations in the human Ca2+-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism

Year: 1993

Type: article

Source: Cell

DOI: 10.1016/0092-8674(93)90617-y

Authors: Martin R. Pollak, Edward M. Brown, Yah-Huei Wu Chou, Steven C. Hebert, Stephen J. Marx, Beat Stelnmann, Tatjana Levi, Christine E. Seidman, J.G. Seidman

Institutions: Brigham and Women's Hospital, Howard Hughes Medical Institute, Harvard University, National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases, University of Zurich

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: W2145930493

FWCI: 34.75

Cites: 27

Cited by: 1,038

Related to: 10