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HARVARD Citation
Caress, J. et al. (2017). Exome sequencing establishes a gelsolin mutation as the cause of inherited bulbar‐onset neuropathy. Muscle & nerve. 56 (5), pp. 1001-1005. [Online].
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Caress, J. et al. (2017). Exome sequencing establishes a gelsolin mutation as the cause of inherited bulbar‐onset neuropathy. Muscle & nerve. 56 (5), pp. 1001-1005. [Online].