Molecular Genetics of Duchenne and Becker Muscular Dystrophy
Author:
Publisher
Elsevier
Reference347 articles.
1. MYOGLOBINÆMIA IN DUCHENNE MUSCULAR DYSTROPHY PATIENTS AND CARRIERS: A NEW ADJUNCT TO CARRIER DETECTION
2. Detailed ordering of markers localizing to the Xq26-Xqter region of the human X chromosome by the use of an interspecific Mus spretus mouse cross.
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1. Casimersen (AMONDYS 45™): An Antisense Oligonucleotide for Duchenne Muscular Dystrophy;Biomedicines;2024-04-20
2. Ixazomib, an oral proteasome inhibitor, exhibits potential effect in dystrophin‐deficient mdx mice;International Journal of Experimental Pathology;2020-12-09
3. Molecular diagnosis of muscular dystrophies;Neuropathology;1998-06
4. Invited review: From dystrophinopathy to sarcoglycanopathy: Evolution of a concept of muscular dystrophy;MUSCLE NERVE;1998
5. From dystrophinopathy to sarcoglycanopathy: Evolution of a concept of muscular dystrophy;Muscle & Nerve;1998-04
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