Campbell, Kevin P.

Top Publications

Top Publications Authored or Co-Authored by "Campbell, Kevin P."

• Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophy

  Nature, Volume 359, No. 6393, Year 1992, Citations 262
• C-terminal titin deletions cause a novel early-onset myopathy with fatal cardiomyopathy

  Annals of Neurology, Volume 61, No. 4, Year 2007, Citations 222
• Primary adhalinopathy: A common cause of autosomal recessive muscular dystrophy of variable severity

  Nature Genetics, Volume 10, No. 2, Year 1995, Citations 197
• Mutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of α-dystroglycan

  American Journal of Human Genetics, Volume 92, No. 3, Year 2013, Citations 170
• Mild congenital muscular dystrophy in two patients with an internally deleted laminin α2-chain

  Human Molecular Genetics, Volume 6, No. 5, Year 1997, Citations 138