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)

Article / Letter to editor

• limb-girdle muscular dystrophy
• Miyoshi muscular dystrophy
• neurology
• neuromuscular disorders

• All authors: Dam, L. ten; Frankhuizen, W.S.; Linssen, W.H.J.P.; Straathof, C.S.; Niks, E.H.; Faber, K.; Fock, A.; Kuks, J.B.; Brusse, E.; Coo, R. de; Voermans, N.; Verrips, A.; Hoogendijk, J.E.; Pol, L. van der; Westra, D.; Visser, M. de; Kooi, A.J. van der; Ginjaar, I.
• Date: 2019-08-31
• Journal: Clinical Genetics
• Volume: 96
• Issue: 2
• Pages: 126 - 133
• DOI: doi:10.1111/cge.13544