DOI:
10.1055/s-00000041
Neuropediatrics
LinksClose Window
References
Vissing J, Barresi R, Witting N. , et al.
A heterozygous 21-bp deletion in CAPN3 causes dominantly inherited limb girdle muscular dystrophy.
Brain 2016;
139 (Pt 8): 2154-2163
Search in:
Access:
We do not assume any responsibility for the contents of the web pages of other providers.