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

Open Access

Peer-reviewed

Research Article

Carlos A. Pantoja-Melendez,

Affiliation Department of Genetics-Research Unit, Institute of Ophthalmology “Conde de Valenciana”, Mexico City, Mexico
⨯
Antonio Miranda-Duarte,

Affiliation Department of Genetics, Instituto Nacional de Rehabilitacion, Mexico City, Mexico
⨯
Bladimir Roque-Ramirez,

Affiliation Pharmacobiology Department, CINVESTAV-Sede Sur, Mexico City, Mexico
⨯
Juan C. Zenteno

* E-mail: jczenteno@institutodeoftalmologia.org

Affiliations Department of Genetics-Research Unit, Institute of Ophthalmology “Conde de Valenciana”, Mexico City, Mexico, Department of Biochemistry, Faculty of Medicine, UNAM, Mexico City, Mexico
⨯

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Homozygosity
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Carrier frequencies
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Heterozygosity
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Mutation detection
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Genomics
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Homozygosity mapping
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Mexican people
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Muscular dystrophies
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