Characterization of MTM1 mutations in 31 Japanese families with myotubular myopathy, including a patient carrying 240 kb deletion in Xq28 without male hypogenitalism - Concepedia

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Characterization of MTM1 mutations in 31 Japanese families with myotubular myopathy, including a patient carrying 240 kb deletion in Xq28 without male hypogenitalism

51

Citations

15

References

2005

Year

Tzung-Chang Tsai, Hideo Horinouchi, S. Noguchi, Narihiro Minami, Kumiko Murayama, Yukiko Hayashi, Ikuya Nonaka, Ichizo Nishino

Neuromuscular Disorders

References

	Year	Citations

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