Published in
Wiley, American Journal of Medical Genetics Part A, 4(158A), p. 772-778, 2012
DOI: 10.1002/ajmg.a.35243
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Recessive RYR1 mutations in a patient with severe congenital nemaline myopathy with ophthalomoplegia identified through massively parallel sequencing
Journal article published in 2012 by
Eri Kondo,
Takafumi Nishimura,
Tomoki Kosho,
Yuji Inaba,
Satomi Mitsuhashi,
Takefumi Ishida,
Atsushi Baba,
Kenichi Koike,
Ichizo Nishino 
,
Ikuya Nonaka,
Toru Furukawa,
Kayoko Saito
,
Ikuya Nonaka,
Toru Furukawa,
Kayoko Saito
This paper was not found in any repository, but could be made available legally by the author.
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