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(1 - 3 of 3)
Autosomal recessive limb-girdle and Miyoshi muscular dystrophies in the Netherlands: The clinical and molecular spectrum of 244 patients
Dam, L. ten; Frankhuizen, W.S.; Linssen, W.H.J.P.; Straathof, C.S.; Niks, E.H.; Faber, K.; ... ; Ginjaar, I. 2019
Autosomal recessive limb-girdle and Miyoshi muscular dystrophies in the Netherlands: The clinical and molecular spectrum of 244 patients
Article / Letter to editor
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Genetic and clinical heterogeneity of RYR1-related myopathies in a cohort of 60 Dutch families with identification of 40 novel mutations
Voermans, N.C.; Jungbluth, H.; Raaphorst, J.; Snoeck, M.; Straathof, C.; Schelhaas, H.J.; ... ; Engelen, B.G.M. van 2012
Genetic and clinical heterogeneity of RYR1-related myopathies in a cohort of 60 Dutch families with identification of 40 novel mutations
Article / Letter to editor
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Germline Mitochondrial DNA Mutations As a Novel First Event in Childhood Myelodysplastic Syndrome
Vries, A. de; Zwaan, C.M.; Beverloo, H.B.; Wagner, A.; Lankester, A.; Boekhorst, P.T.; ... ; Heuvel, M.M. van den 2011
Germline Mitochondrial DNA Mutations As a Novel First Event in Childhood Myelodysplastic Syndrome
Article / Letter to editor
metadata only