Issn Print: 0148-639X
Publication Date: 2017/11/01
Exome sequencing establishes a gelsolin mutation as the cause of inherited bulbar‐onset neuropathy
James B. Caress; Janel O. Johnson; Yevgeniya A. Abramzon; Gregory A. Hawkins; J. Raphael Gibbs; Elizabeth A. Sullivan; Chamanpreet S. Chahal; Bryan J. Traynor
Author Information: Department of Neurology, Wake Forest School of Medicine
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