Associated Papers
Leprosy and the human genome.
Misch EA et al.
Microbiology and Molecular Biology Reviews : Mmbr, 2010
Clinical and molecular study in congenital muscular dystrophy with partial laminin alpha 2 (LAMA2) deficiency.
Tezak Z et al.
Human Mutation, 2003
Association of a missense mutation of the laminin alpha2 gene with tuberculoid type of leprosy in Indonesian patients.
Wibawa T et al.
Tropical Medicine & International Health : Tm & Ih, 2002
Congenital muscular dystrophy with primary laminin alpha2 (merosin) deficiency presenting as inflammatory myopathy.
Pegoraro E et al.
Annals of Neurology, 1996
Select a paper to view details