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Infantile Onset Hypertrophic Cardiomyopathy Secondary to PRKAG2 Gene Mutation is Associated with Poor Prognosis
Hypertrophic cardiomyopathy (HCM) is the second most prevalent form of cardiomyopathy in children. The etiology of the HCM is heterogeneous, so is the age of onset of symptoms. The HCM associated with metabolic disorders and genetic syndromes presents early in childhood. There are very few case repo...
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| Pubblicato in: | J Pediatr Genet |
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| Autori principali: | , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Georg Thieme Verlag KG
2018
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| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6234042/ https://ncbi.nlm.nih.gov/pubmed/30430036 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1055/s-0038-1657763 |
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