Original language | English |
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Pages (from-to) | 88-89 |
Journal | Neuromuscular Disorders |
Volume | 24 |
DOIs | |
Publication status | Published - 2014 |
Compound heterozygous mutations of the TNXB gene cause primary myopathy.
N.C. Voermans, K.H.L. Gerrits, B.G. van Engelen, A. de Haan
Research output: Contribution to Journal › Article › Academic › peer-review