bibliographic entry 7477177 [be/7477177]
https://w3id.org/oc/corpus/be/7477177

is a
content
  • Mata, IF, Jang, Y, Kim, C-H, Hanna, DS, Dorschner, MO, Samii, A, Agarwal, P, Roberts, JW, Klepitskaya, O, Shprecher, DR, Chung, KA, Factor, SA, Espay, AJ, Revilla, FJ, Higgins, DS, Litvan, I, Leverenz, JB, Yearout, D, Inca-Martinez, M, Martinez, E, Thompson, TR, Cholerton, BA, Hu, S-C, Edwards, KL, Kim, K-S, Zabetian, CP. 2015, The RAB39B p.G192R mutation causes x-linked dominant parkinson’s disease, Molecular Neurodegeneration, 10, 50, DOI: 10.1186/s13024-015-0045-4, PMID: 26399558
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