Autosomal dominant hypoparathyroidism caused by germline mutation in GNA11: phenotypic and molecular characterization. [electronic resource]
Producer: 20150112Description: E1774-83 p. digitalISSN:- 1945-7197
- Adolescent
- Adult
- Bone Development -- genetics
- Child
- Child, Preschool
- Family Health
- Female
- GTP-Binding Protein alpha Subunits -- genetics
- Genome-Wide Association Study
- Germ-Line Mutation -- genetics
- Heterozygote
- Humans
- Hypercalciuria -- genetics
- Hypocalcemia -- genetics
- Hypoparathyroidism -- congenital
- Male
- Middle Aged
- Pedigree
- Phenotype
- Young Adult
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Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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