Published in
Oxford University Press (OUP), Journal of Neuropathology and Experimental Neurology, 6(68), p. 701-707, 2009
DOI: 10.1097/nen.0b013e3181a7f703
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Defective Myotilin Homodimerization Caused by a Novel Mutation in MYOT Exon 9 in the First Japanese Limb Girdle Muscular Dystrophy 1A Patient
Journal article published in 2009 by
Sherine Shalaby,
Hiroaki Mitsuhashi,
Chie Matsuda,
Narihiro Minami,
Satoru Noguchi,
Ikuya Nonaka,
Ichizo Nishino 
,
Yukiko K. Hayashi
,
Yukiko K. Hayashi
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