Rare intronic mutation between Exon 62 and 63...

Neuromuscular Disorders 2020 / 6

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, R
How much do you like this book?
What’s the quality of the file?
Download the book for quality assessment
What’s the quality of the downloaded files?
Journal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2020.06.003
Date:
June, 2020
File:
PDF, 2.73 MB
2020
Conversion to is in progress
Conversion to is failed