A
tropomyosin-receptor kinase-fused
gene mutation associates with vacuolar myopathy
Neurol Genet
.
2018 Nov 7;4(6):e287.
doi: 10.1212/NXG.0000000000000287.
eCollection 2018 Dec.
Authors
Nicolas N Madigan
1
,
Jennifer A Tracy
1
,
William J Litchy
1
,
Zhiyv Niu
1
,
Chunhua Chen
1
,
Kun Ling
1
,
Margherita Milone
1
Affiliation
1
Department of Neurology (N.N.M., J.A.T., W.J.L., M.M.), Department of Laboratory Medicine and Pathology (Z.N.), Department of Clinical Genomics (Z.N.), and Department of Biochemistry & Molecular Biology (C.C., K.L.), Mayo Clinic, Rochester, MN.
PMID:
30643850
PMCID:
PMC6317988
DOI:
10.1212/NXG.0000000000000287
No abstract available