Autosomal dominant hypocalcaemia caused by a Ca2+-sensing receptor gene mutation.
| Autor: | Pollak, Martin R., Brown, Edward M., Estep, Herschel L., McLaine, Peter N., Kifor, Olga, Park, Ji, Hebert, Steven C., Seidman, Christine E., Seidman, J. G. |
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| Zdroj: | Nature Genetics; Nov1994, Vol. 8 Issue 3, p303-307, 5p |
| Databáze: | Complementary Index |
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