bibliographicCitation |
Braathen GJ, Høyer H, Busk ØL, Tveten K, Skjelbred CF, Russell MB. Variants in the genesDCTN2,DNAH10,LRIG3,andMYO1Aare associated with intermediate Charcot–Marie–Tooth disease in a Norwegian family. Acta Neurol Scand. 2015 Oct 12;134(1):67–75. doi: 10.1111/ane.12515. |