Associated Papers
A rare case of arrhythmogenic right ventricular cardiomyopathy associated with LAMA2 mutation: A case report and literature review.
Wang Y et al.
Frontiers in Medicine, 2022
A single point mutation in the LN domain of LAMA2 causes muscular dystrophy and peripheral amyelination.
Patton BL et al.
Journal of Cell Science, 2008
Congenital muscular dystrophy with primary partial laminin alpha2 chain deficiency: molecular study.
He Y et al.
Neurology, 2001
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