Reply: Dominant LGMD2A: alternative diagnosis or hidden digenism?

Affiliations

¹ Copenhagen Neuromuscular Center, Department of Neurology, University of Copenhagen, Denmark vissing@rh.dk.
² Department of Clinical Genetics, Rigshospitalet, University of Copenhagen, Denmark.

Comment

John Vissing et al. Brain. 2017 Feb.

. 2017 Feb;140(2):e8.

doi: 10.1093/brain/aww283. Epub 2016 Nov 15.

¹ Copenhagen Neuromuscular Center, Department of Neurology, University of Copenhagen, Denmark vissing@rh.dk.
² Department of Clinical Genetics, Rigshospitalet, University of Copenhagen, Denmark.

No abstract available

Comment on

A heterozygous 21-bp deletion in CAPN3 causes dominantly inherited limb girdle muscular dystrophy.
Vissing J, Barresi R, Witting N, Van Ghelue M, Gammelgaard L, Bindoff LA, Straub V, Lochmüller H, Hudson J, Wahl CM, Arnardottir S, Dahlbom K, Jonsrud C, Duno M. Vissing J, et al. Brain. 2016 Aug;139(Pt 8):2154-63. doi: 10.1093/brain/aww133. Epub 2016 Jun 3. Brain. 2016. PMID: 27259757
Dominant LGMD2A: alternative diagnosis or hidden digenism?
Sáenz A, López de Munain A. Sáenz A, et al. Brain. 2017 Feb;140(2):e7. doi: 10.1093/brain/aww281. Epub 2016 Nov 5. Brain. 2017. PMID: 27818383 No abstract available.