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PFN2 and GAMT as common molecular determinants of axonal Charcot-Marie-Tooth disease
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| Abstract |
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English
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Journal of neurology, neurosurgery and psychiatry. - London | |
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London : 2018
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0022-3050
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89:8(2018), p. 870-878
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000442475000020
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29449460
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VIB-Integrated European -omics research project for diagnosis and therapy in rare neuromuscular and neurodegenerative diseases (NEUROMICS).
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Publications with a UAntwerp address
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| Creation |
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08.10.2018
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| Last edited |
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19.02.2020
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