MicroRNAs as serum biomarkers in Becker muscular dystrophy
D Gagliardi, M Rizzuti, R Brusa… - Journal of Cellular …, 2022 - Wiley Online Library
Becker muscular dystrophy (BMD) is an X‐linked neuromuscular disorder due to mutation in
the DMD gene, encoding dystrophin. Despite a wide clinical variability, BMD is …
the DMD gene, encoding dystrophin. Despite a wide clinical variability, BMD is …
MicroRNAs as serum biomarkers in Becker muscular dystrophy
D Gagliardi, M Rizzuti, R Brusa… - Journal of cellular …, 2022 - pubmed.ncbi.nlm.nih.gov
Becker muscular dystrophy (BMD) is an X-linked neuromuscular disorder due to mutation in
the DMD gene, encoding dystrophin. Despite a wide clinical variability, BMD is …
the DMD gene, encoding dystrophin. Despite a wide clinical variability, BMD is …
MicroRNAs as serum biomarkers in Becker muscular dystrophy
D Gagliardi, M Rizzuti, R Brusa, M Ripolone… - … OF CELLULAR AND …, 2022 - air.unimi.it
Becker muscular dystrophy (BMD) is an X-linked neuromuscular disorder due to mutation in
the DMD gene, encoding dystrophin. Despite a wide clinical variability, BMD is …
the DMD gene, encoding dystrophin. Despite a wide clinical variability, BMD is …
MicroRNAs as serum biomarkers in Becker muscular dystrophy
D Gagliardi, M Rizzuti, R Brusa… - Journal of Cellular …, 2022 - search.proquest.com
Becker muscular dystrophy (BMD) is an X‐linked neuromuscular disorder due to mutation in
the DMD gene, encoding dystrophin. Despite a wide clinical variability, BMD is …
the DMD gene, encoding dystrophin. Despite a wide clinical variability, BMD is …
MicroRNAs as serum biomarkers in Becker muscular dystrophy.
D Gagliardi, M Rizzuti, R Brusa, M Ripolone… - Journal of Cellular …, 2022 - europepmc.org
Becker muscular dystrophy (BMD) is an X‐linked neuromuscular disorder due to mutation in
the DMD gene, encoding dystrophin. Despite a wide clinical variability, BMD is …
the DMD gene, encoding dystrophin. Despite a wide clinical variability, BMD is …
[HTML][HTML] MicroRNAs as serum biomarkers in Becker muscular dystrophy
D Gagliardi, M Rizzuti, R Brusa… - Journal of Cellular …, 2022 - ncbi.nlm.nih.gov
Becker muscular dystrophy (BMD) is an X‐linked neuromuscular disorder due to mutation in
the DMD gene, encoding dystrophin. Despite a wide clinical variability, BMD is …
the DMD gene, encoding dystrophin. Despite a wide clinical variability, BMD is …
[PDF][PDF] MicroRNAs as serum biomarkers in Becker muscular dystrophy
D Gagliardi, M Rizzuti, R Brusa, M Ripolone, S Zanotti… - 2022 - air.unimi.it
Becker muscular dystrophy (BMD) is an X-linked neuromuscular disorder due to mutation in
the DMD gene, encoding dystrophin. Despite a wide clinical variability, BMD is …
the DMD gene, encoding dystrophin. Despite a wide clinical variability, BMD is …