Exome sequencing establishes a gelsolin mutation as the cause of inherited bulbar-onset neuropathy.
Caress, James B. MD *,1; Johnson, Janel O. PhD 2; Abramzon, Yevgeniya A. BS 3,4; Hawkins, Gregory A. PhD 5; Gibbs, J. Raphael PhD 6,7; Sullivan, Elizabeth A. MD 8; Chahal, Chamanpreet S. MD 9; Traynor, Bryan J. MD, PhD 2
Muscle & Nerve.
56(5):1001-1005, November 2017.
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