Hypoparathyroidism by glial cells missing B mutations (Q98058)
From determinar.ia.br - Determine suas informações
GCMB is a transcription factor which have essential role in the development of parathyroid hormone. Both autosomal dominant and recessive forms of familial hypoparathyroidism due to mutations in GCMB gene have been reported. (OMIM #146200)
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_153432885 |
||
| English | Hypoparathyroidism by glial cells missing B mutations |
GCMB is a transcription factor which have essential role in the development of parathyroid hormone. Both autosomal dominant and recessive forms of familial hypoparathyroidism due to mutations in GCMB gene have been reported. (OMIM #146200) |
Statements
CID11:ID_153432885
0 references
dki-india-ID_153432885
0 references
Concluído
0 references
15 August 2026
0 references
