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Werdnig‐Hoffmann disease and chronic distal spinal muscular atrophy with apparent autosomal dominant inheritance
Kevin B. Boylan, David R. Cornblath
Neurology
Research output
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Contribution to journal
›
Article
›
peer-review
7
Scopus citations
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Dive into the research topics of 'Werdnig‐Hoffmann disease and chronic distal spinal muscular atrophy with apparent autosomal dominant inheritance'. Together they form a unique fingerprint.
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Medicine & Life Sciences
Spinal Muscular Atrophy
100%
Chronic Disease
56%
Motor Neuron Disease
48%
Denervation
41%
Electromyography
38%
Fathers
37%
Siblings
35%
Atrophy
33%
Signs and Symptoms
33%
Leg
31%
Hand
29%
Extremities
28%
Mothers
24%