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Spontaneous Coronary Artery Dissection: A Rare Manifestation of Alport Syndrome
Alport syndrome (AS) is a genetic disorder due to inheritance of genetic mutations which lead to production of abnormal type IV collagen. AS has been associated with renal, auditory, and ocular diseases due to the presence of abnormal alpha chains of type IV collagen in the glomerulus, cochlea, corn...
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| Pubblicato in: | Case Rep Cardiol |
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| Autori principali: | , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Hindawi
2017
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5573093/ https://ncbi.nlm.nih.gov/pubmed/28884028 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2017/1705927 |
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