A missense glial cells missing homolog B (GCMB) mutation, Asn502His, causes autosomal dominant hypoparathyroidism. (Q42170326)
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scientific article published on 12 May 2010
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | A missense glial cells missing homolog B (GCMB) mutation, Asn502His, causes autosomal dominant hypoparathyroidism. |
scientific article published on 12 May 2010 |
Statements
A missense glial cells missing homolog B (GCMB) mutation, Asn502His, causes autosomal dominant hypoparathyroidism (English)
Samantha M Mirczuk
M Andrew Nesbit
Carl Fratter
Jeremy Allgrove
Caroline Brain