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Rare intronic mutation between Exon 62 and 63 (c.9225-285A>G) of the dystrophin gene associated with atypical BMD phenotype: a case report
Schüssler, SC, Gerhalter, T, Abicht, A, Müller-Felber, W, Nagel, AM, Trollmann, RJournal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2020.06.003
Date:
June, 2020
File:
PDF, 2.73 MB
2020