Sleep Issues in Motor Neuron Diseases
Author:
Publisher
Springer International Publishing
Link
http://link.springer.com/content/pdf/10.1007/978-3-319-73068-4_3
Reference54 articles.
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4. Rudnik-Schoneborn S, Deden F, Eggermann K, Eggermann T, Wieczorek D, Sellhaus B, et al. Autosomal dominant spinal muscular atrophy with lower extremity predominance: a recognizable phenotype of BICD2 mutations. Muscle Nerve. 2016;54(3):496–500.
5. Tsurusaki Y, Saitoh S, Tomizawa K, Sudo A, Asahina N, Shiraishi H, et al. A DYNC1H1 mutation causes a dominant spinal muscular atrophy with lower extremity predominance. Neurogenetics. 2012;13(4):327–32.
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