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A novel DMD splicing mutation found in a family responsible for X-linked dilated cardiomyopathy with hyper-CKemia
This study was aimed to detect a new mutation responsible for X-linked dilated cardiomyopathy with hyper-CKemia. We studied a proband who presented with cardiac symptoms with hyper-CKemia, but no clinical skeletal involvement in physical examination, laboratory tests, electromyography, echocardiogra...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6024070/ https://www.ncbi.nlm.nih.gov/pubmed/29901616 http://dx.doi.org/10.1097/MD.0000000000011074 |