Ontology highlight
ABSTRACT:
INSTRUMENT(S): TripleTOF 6600
ORGANISM(S): Mus Musculus (ncbitaxon:10090)
SUBMITTER: Karen Colwill
PROVIDER: MSV000089845 | MassIVE | Thu Jul 07 12:03:00 BST 2022
SECONDARY ACCESSION(S): PXD035164
REPOSITORIES: MassIVE
Sarikaya Ege E Sabha Nesrin N Volpatti Jonathan J Pannia Emanuela E Maani Nika N Gonorazky Hernan D HD Celik Alper A Liang Yijng Y Onofre-Oliveira Paula P Dowling James J JJ
Disease models & mechanisms 20220725 7
X-linked myotubular myopathy (XLMTM) is a severe monogenetic disorder of the skeletal muscle. It is caused by loss-of-expression/function mutations in the myotubularin (MTM1) gene. Much of what is known about the disease, as well as the treatment strategies, has been uncovered through experimentation in pre-clinical models, particularly the Mtm1 gene knockout mouse line (Mtm1 KO). Despite this understanding, and the identification of potential therapies, much remains to be understood about XLMTM ...[more]