Pages that link to "Q33608787"

The following pages link to Limb-girdle muscular dystrophies: where next after six decades from the first proposal (Review). (Q33608787):

Displaying 11 items.

• Homozygous nonsense mutation in SGCA is a common cause of limb-girdle muscular dystrophy in Assiut, Egypt (Q33751724) (← links)
• Epidemiological and Molecular Characterization of a Mexican Population Isolate with High Prevalence of Limb-Girdle Muscular Dystrophy Type 2A Due to a Novel Calpain-3 Mutation. (Q36254120) (← links)
• Concise review: mesoangioblast and mesenchymal stem cell therapy for muscular dystrophy: progress, challenges, and future directions (Q38267714) (← links)
• Quality of life in adult patients with limb-girdle muscular dystrophies (Q47286333) (← links)
• LGMD2E is the most common type of sarcoglycanopathies in the Iranian population (Q47791677) (← links)
• Muscle Cells Fix Breaches by Orchestrating a Membrane Repair Ballet. (Q52373051) (← links)
• Bethlem myopathy in a Portuguese patient - case report. (Q54108945) (← links)
• Identification of a Novel Mutation in the Titin Gene in a Chinese Family with Limb-Girdle Muscular Dystrophy 2J. (Q54245073) (← links)
• Genetic landscape and novel disease mechanisms from a large LGMD cohort of 4656 patients (Q60047970) (← links)
• The Limb-Girdle Muscular Dystrophies: Is Treatment on the Horizon? (Q64044289) (← links)
• The Latin American experience with a next generation sequencing genetic panel for recessive limb-girdle muscular weakness and Pompe disease (Q92605287) (← links)