A tropomyosin-receptor kinase-fused gene mutation associates with vacuolar myopathy

Nicolas N. Madigan, Jennifer A. Tracy, William J Litchy, Zhiyv Niu, Chunhua Chen, Kun Ling, Margherita Milone

Research output: Contribution to journal › Article

2 Citations (Scopus)
Original languageEnglish (US)
Article numbere287
JournalNeurology: Genetics
Volume4
Issue number6
DOIs
StatePublished - Dec 1 2018

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Mutation
Genes
tropomyosin kinase
Vacuolar myopathy

ASJC Scopus subject areas

  • Clinical Neurology
  • Genetics(clinical)

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A tropomyosin-receptor kinase-fused gene mutation associates with vacuolar myopathy. / Madigan, Nicolas N.; Tracy, Jennifer A.; Litchy, William J; Niu, Zhiyv; Chen, Chunhua; Ling, Kun; Milone, Margherita.

In: Neurology: Genetics, Vol. 4, No. 6, e287, 01.12.2018.

Research output: Contribution to journal › Article

Madigan, NN, Tracy, JA, Litchy, WJ, Niu, Z, Chen, C, Ling, K & Milone, M 2018, 'A tropomyosin-receptor kinase-fused gene mutation associates with vacuolar myopathy', Neurology: Genetics, vol. 4, no. 6, e287. https://doi.org/10.1212/NXG.0000000000000287
Madigan NN, Tracy JA, Litchy WJ, Niu Z, Chen C, Ling K et al. A tropomyosin-receptor kinase-fused gene mutation associates with vacuolar myopathy. Neurology: Genetics. 2018 Dec 1;4(6). e287. https://doi.org/10.1212/NXG.0000000000000287
Madigan, Nicolas N. ; Tracy, Jennifer A. ; Litchy, William J ; Niu, Zhiyv ; Chen, Chunhua ; Ling, Kun ; Milone, Margherita. / A tropomyosin-receptor kinase-fused gene mutation associates with vacuolar myopathy. In: Neurology: Genetics. 2018 ; Vol. 4, No. 6.
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