Molecular Diagnosis of Duchenne/Becker muscular dystrophy in a family with no pathological antecedents of the disease

Molecular Diagnosis of Duchenne/Becker muscular dystrophy in a family with no pathological antecedents of the disease

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<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...

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Bibliographic Details
Main Authors: Ivonne Martín Hernández, Alejandro Ariosa Olea, Mariesky Zayas Guillot, Tatiana Zaldívar Vaillant, Celia Rosa Soto Pérez-Stable
Format: Article
Language:Spanish
Published: Centro Provincial de Información de Ciencias Médicas. Cienfuegos 2018-10-01
Series:Medisur
Subjects:
distrofia muscular de duchenne
deleción cromosómica
patología molecular
enfermedades genéticas ligadas al cromosoma x
Online Access:http://www.medisur.sld.cu/index.php/medisur/article/view/3847

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http://www.medisur.sld.cu/index.php/medisur/article/view/3847

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