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Journal article
Schuessler, S. C.; Gerhalter, T.; Abicht, A.; Müller-Felber, W.; Nagel, A. M. and Trollmann, R.
(2020):
p report Rare intronic mutation between Exon 62 and 63 (c.9225-285A > G) of the dystrophin gene associated with atypical BMD phenotype.
In: Neuromuscular Disorders, Vol. 30, No. 8: pp. 680-684