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Left Ventricular Noncompaction in a Family with Lamin A/C Gene Mutation
Left ventricular noncompaction is a rare type of cardiomyopathy, the genetics of which are poorly understood to date. Lamin A/C gene mutations have been associated with dilated cardiomyopathy and diseases of the conduction system, but rarely in left ventricular noncompaction cardiomyopathy. This rep...
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| Foilsithe in: | Tex Heart Inst J |
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| Main Authors: | , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
Texas Heart® Institute, Houston
2015
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4378052/ https://ncbi.nlm.nih.gov/pubmed/25873806 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.14503/THIJ-13-3843 |
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