Neonatal severe hyperparathyroidism secondary to a novel homozygous CASR gene mutation.
- DOI
- 10.11138/ccmbm/2017.14.3.354
- Published
- 2017 Sep-Dec
- Container
- Clinical cases in mineral and bone metabolism : the official journal of the Italian Society of Osteoporosis, Mineral Metabolism, and Skeletal Diseases
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.11138/ccmbm/2017.14.3.354,
title = {Neonatal severe hyperparathyroidism secondary to a novel homozygous CASR gene mutation.},
author = {Ahmad N and Bahasan M and Al-Ghamdi BAA and Al-Enizi HF and Al-Zahrani AS},
year = {2017},
journal = {Clinical cases in mineral and bone metabolism : the official journal of the Italian Society of Osteoporosis, Mineral Metabolism, and Skeletal Diseases},
doi = {10.11138/ccmbm/2017.14.3.354},
url = {https://doi.org/10.11138/ccmbm/2017.14.3.354}
}RIS
TY - JOUR TI - Neonatal severe hyperparathyroidism secondary to a novel homozygous CASR gene mutation. AU - Ahmad N AU - Bahasan M AU - Al-Ghamdi BAA AU - Al-Enizi HF AU - Al-Zahrani AS PY - 2017 JO - Clinical cases in mineral and bone metabolism : the official journal of the Italian Society of Osteoporosis, Mineral Metabolism, and Skeletal Diseases DO - 10.11138/ccmbm/2017.14.3.354 UR - https://doi.org/10.11138/ccmbm/2017.14.3.354 ER -
APA
N, A., M, B., BAA, A., HF, A., & AS, A. (2017). Neonatal severe hyperparathyroidism secondary to a novel homozygous CASR gene mutation.. Clinical cases in mineral and bone metabolism : the official journal of the Italian Society of Osteoporosis, Mineral Metabolism, and Skeletal Diseases. https://doi.org/10.11138/ccmbm/2017.14.3.354
Source records
- pubmed · retrieved 2026-09-27T14:16:15.223Z