Molecular Diagnosis of Duchenne/Becker muscular dystrophy in a family with no pathological antecedents of the disease
<p><strong>Foundation</strong>: Duchenne and Becker muscular dystrophies are progressive neuromuscular diseases with a pattern of recessive inherited link to chromosome X and caused by mutations in the gene which codifies for dystrophin. The study of possible carriers in affected...
Main Authors: | Ivonne Martín Hernández, Alejandro Ariosa Olea, Mariesky Zayas Guillot, Tatiana Zaldívar Vaillant, Celia Rosa Soto Pérez-Stable |
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Format: | Article |
Language: | Spanish |
Published: |
Centro Provincial de Información de Ciencias Médicas. Cienfuegos
2018-10-01
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Series: | Medisur |
Subjects: | |
Online Access: | http://www.medisur.sld.cu/index.php/medisur/article/view/3847 |
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