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Hereditary Hyperferritinemia-Cataract Syndrome in 3 Generations of a Family in East Tennessee
Hereditary hyperferritinemia and cataracts syndrome (HHCS) without iron overload is a syndrome first identified less than 3 decades ago. While investigators have dissected the gene where several responsible mutations reside, it remains a relatively unknown genetic disorder to clinicians. The result...
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| Vydáno v: | Case Rep Hematol |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Hindawi
2020
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7271056/ https://ncbi.nlm.nih.gov/pubmed/32547795 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2020/2837573 |
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