Neonatal severe hyperparathyroidism secondary to a novel homozygous CASR gene mutation.
| Autor: | Ahmad, Noman1 anoman@kfshrc.edu.sa, Bahasan, Mona1, Abdullah Al-Ghamdi, Balgees Abdulhadi1, Al-Enizi, Halah Faleh2, Al-Zahrani, Ali Saeed2 |
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| Zdroj: | Clinical Cases in Mineral & Bone Metabolism. Oct-Dec2017, Vol. 14 Issue 3, p354-358. 5p. |
| Databáze: | Academic Search Ultimate |
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