LAMA2-Related Dystrophies: Clinical Phenotypes, Disease Biomarkers, and Clinical Trial Readiness
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DOI: 10.3389/fnmol.2020.00123
Abstract: Mutations in the LAMA2 gene affect the production of the α2 subunit of laminin-211 (= merosin) and result in either partial or complete laminin-211 deficiency. Complete merosin deficiency is typically associated with a more severe… read more here.
Keywords: lama2 related; outcome measures; muscle; lama2 rds ... See more keywords