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Molecular Analysis Confirms that FKRP-Related Disorders are Underdiagnosed in Mexican Patients with Neuromuscular Diseases.
Neuropediatrics. 2017 Dec;48(6):442-450. doi: 10.1055/s-0037-1607054. Epub 2017 Oct 24.
Neuropediatrics. 2017.
PMID: 29065428
No abstract available.
Predominance of Dystrophinopathy Genotypes in Mexican Male Patients Presenting as Muscular Dystrophy with A Normal Multiplex Polymerase Chain Reaction DMD Gene Result: A Study Including Targeted Next-Generation Sequencing.
Alcántara-Ortigoza MA, Reyna-Fabián ME, González-Del Angel A, Estandia-Ortega B, Bermúdez-López C, Cruz-Miranda GM, Ruíz-García M.
Alcántara-Ortigoza MA, et al. Among authors: bermudez lopez c.
Genes (Basel). 2019 Oct 29;10(11):856. doi: 10.3390/genes10110856.
Genes (Basel). 2019.
PMID: 31671740
Free PMC article.
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Germinal mosaicism in a sample of families with Duchenne/Becker muscular dystrophy with partial deletions in the DMD gene.
Bermúdez-López C, García-de Teresa B, González-del Angel A, Alcántara-Ortigoza MA.
Bermúdez-López C, et al.
Genet Test Mol Biomarkers. 2014 Feb;18(2):93-7. doi: 10.1089/gtmb.2013.0384. Epub 2013 Nov 16.
Genet Test Mol Biomarkers. 2014.
PMID: 24236769
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