The Ca(2+)-sensing receptor gene (PCAR1) mutation T151M in isolated autosomal dominant hypoparathyroidism.

Løvlie, R

The Ca(2+)-sensing receptor gene (PCAR1) mutation T151M in isolated autosomal dominant hypoparathyroidism. [electronic resource] - Human genetics Aug 1996 - 129-33 p. digital

Publication Type: Journal Article

0340-6717

10.1007/s004390050174 doi


Amino Acid Sequence
Base Sequence
Child
Chromosome Mapping
Chromosomes, Human, Pair 3--genetics
DNA, Complementary--genetics
Female
Genes, Dominant
Genetic Linkage
Genetic Markers
Humans
Hypoparathyroidism--genetics
Male
Middle Aged
Molecular Sequence Data
Pedigree
Point Mutation
Polymorphism, Single-Stranded Conformational
Receptors, Calcium-Sensing
Receptors, Cell Surface--genetics