Novel truncating mutations of
MYO18B
causing congenital myopathy in a Swiss patient
Neurol Genet
.
2020 Jun 9;6(4):e458.
doi: 10.1212/NXG.0000000000000458.
eCollection 2020 Aug.
Authors
Violeta Mihaylova
1
,
Fabian Chablais
1
,
Yvan Herenger
1
,
Roland Spiegel
1
,
Hans Heinrich Jung
1
Affiliation
1
Department of Neurology (V.M., H.H.J.), University Hospital and University of Zurich; and Genetica (F.C., Y.H., R.S.), Human Genetics and Genetic Counselling Unit, Zurich, Switzerland.
PMID:
32637634
PMCID:
PMC7323478
DOI:
10.1212/NXG.0000000000000458
No abstract available