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Neuromuscular Disorders
Volume 19, Issue 12
, Pages
849-852
, December 2009
Myelin protein zero Val102fs mutation manifesting with isolated spinal root hypertrophy
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PII: S0960-8966(09)00617-8
doi: 10.1016/j.nmd.2009.09.004
© 2009 Elsevier B.V. All rights reserved.
« Previous
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Neuromuscular Disorders
Volume 19, Issue 12
, Pages
849-852
, December 2009
