facioscapulohumeral muscular dystrophy (FSHD)

news

New muscular dystrophy treatment shows promise in pre-clinical trials

30 June 2020 | By Victoria Rees (Drug Target Review)

A group of researchers has used locked nucleic acid gapmer antisense oligonucleotides to treat facioscapulohumeral muscular dystrophy in cells and mice.

news

Using CRISPR-Cas9 to identify new gene drug targets

26 March 2020 | By Victoria Rees (Drug Target Review)

Researchers have used CRISPR-Cas9 to screen the genome for possible targets that could be used in potential treatments for muscular dystrophy.

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facioscapulohumeral muscular dystrophy (FSHD)

New muscular dystrophy treatment shows promise in pre-clinical trials

Using CRISPR-Cas9 to identify new gene drug targets