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Carbonic Anhydrase II Deficiency: A Rare Case of Severe Obstructive Sleep Apnea
The term osteopetrosis describes a group of rare hereditary diseases of the skeleton, characterized by an increase in bone density, caused by a defect in the development or function of osteoclasts. It comprises a clinically and genetically heterogeneous conditions ranging from infantile onset life-t...
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| 出版年: | Front Pediatr |
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| 主要な著者: | , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Frontiers Media S.A.
2018
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6079206/ https://ncbi.nlm.nih.gov/pubmed/30109220 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fped.2018.00213 |
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