Ersin Tan

Mutations in a Gene Encoding a Novel SH3/TPR Domain Protein Cause Autosomal Recessive Charcot-Marie-Tooth Type 4C Neuropathy

Jan Senderek, Carsten Bergmann, Claudia Stendel et al. · The American Journal of Human Genetics · 2003 · 212 citations · Full text

Life Sciences, Genetics, Molecular Genetics +10

Mutations in <i>GDAP1</i>

Eva Nelis, Peter Van den Bergh, Marie‐Claude Belpaire‐Dethiou et al. · Neurology · 2002 · 157 citations

Life Sciences, Genetics, Molecular Genetics +14

A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in Turkey

Pervin Dinçer, France Leturcq, Isabelle Richard et al. · Annals of Neurology · 1997 · 120 citations

Medicine, Genetics, Molecular Genetics +15

The spectrum of mutations causing end-plate acetylcholinesterase deficiency

Kinji Ohno, Andrew G. Engel, Joan M. Brengman et al. · Annals of Neurology · 2000 · 120 citations

Life Sciences, Biochemistry, Neuroscience +13

Late onset muscular dystrophy with cerebral white matter changes due to partial merosin deficiency

Ersin Tan, Haluk Topaloğlu, Caroline A. Sewry et al. · Neuromuscular Disorders · 1997 · 79 citations

Medicine, Neurology, Neuroscience +16