Variation in SIPA1L2 is correlated with phenotype modification in Charcot- Marie- Tooth disease type 1A.

Tao, Feifei; Beecham, Gary W; Rebelo, Adriana P; Svaren, John; Blanton, Susan H; Moran, John J; Lopez-Anido, Camila; Morrow, Jasper M; Abreu, Lisa; Rizzo, Devon; Kirk, Callyn A; Wu, Xingyao; Feely, Shawna; Verhamme, Camiel; Saporta, Mario A; Herrmann, David N; Day, John W; Sumner, Charlotte J; Lloyd, Thomas E; Li, Jun; Yum, Sabrina W; Taroni, Franco; Baas, Frank; Choi, Byung-Ok; Pareyson, Davide; Scherer, Steven S; Reilly, Mary M; Shy, Michael E; Züchner, Stephan.
Ann Neurol; 85(3): 316-330, 2019 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-30706531

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