| Original language | English |
|---|---|
| Title of host publication | World Muscle Society 2016 |
| Publication status | Published - 2016 |
A novel homozygous frameshift deletion in the SH3TC2 gene in a patient with Charcot-Marie-Tooth (CMT) type 4C and severe ataxia
Research output: Chapter in Book/Report/Conference proceeding › Conference Contribution (Conference Proceeding)