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Keyword [Marie-Tooth disease type 2D]
Result: 1 - 2 | Page: 1 of 1
1.
The Study Of Clinical Characteristics And Glycyl-tRNA Synthetase Gene Mutations In Adolescent-onset Myoatrophy Of Bilateral Distal Upper Extremities With Knee-jerk Hyperreflexia
2.
Glycyl-tRNA synthetase mutations cause Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V: A potentially novel disease mechanism for human peripheral neuropathies
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