Phenotype of a patient with recessive centronuclear myopathy and a novel BIN1 mutation - Archive ouverte HAL Access content directly
Journal Articles Neurology Year : 2010
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hal-04087155 , version 1 (02-05-2023)

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K Claeys, T Maisonobe, Johann Böhm, Jocelyn Laporte, M Hezode, et al.. Phenotype of a patient with recessive centronuclear myopathy and a novel BIN1 mutation. Neurology, 2010, 74 (6), pp.519-521. ⟨10.1212/WNL.0b013e3181cef7f9⟩. ⟨hal-04087155⟩
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