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Brain : a Journal of Neurology|February 1, 2013
Recessive MYL2 mutations cause infantile type I muscle fibre disease and cardiomyopathyMarian A J Weterman, Peter G Barth, Karin Y van Spaendonck-Zwarts, et al.Brain : a Journal of Neurology|October 1, 1996
The clinical spectrum of limb girdle muscular dystrophy. A survey in The NetherlandsA J van der Kooi, P G Barth, H F Busch, et al.Brain : a Journal of Neurology|October 19, 2010
Clinical, neuroradiological and genetic findings in pontocerebellar hypoplasiaYasmin Namavar, Peter G Barth, Paul R Kasher, et al.Orphanet Journal of Rare Diseases|February 15, 2014
EXOSC3 mutations in pontocerebellar hypoplasia type 1: novel mutations and genotype-phenotype correlationsVeerle Rc Eggens, Peter G Barth, Jikke-Mien F Niermeijer, et al.Nature Genetics|August 20, 2008
tRNA splicing endonuclease mutations cause pontocerebellar hypoplasiaBirgit S Budde, Yasmin Namavar, Peter G Barth, et al.Pageof 30