ICGNMD
@icgnmd.bsky.social
54 followers
27 following
8 posts
We are the International Centre for Genomic Medicine in Neuromuscular Diseases, we aim to grow knowledge about the global causes of inherited neuromuscular diseases and promote inclusion in research. Welcome!
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ICGNMD
@icgnmd.bsky.social
· Feb 24
Biallelic variants in RYR1 and STAC3 are predominant causes of King-Denborough Syndrome in an African cohort - European Journal of Human Genetics
European Journal of Human Genetics - Biallelic variants in RYR1 and STAC3 are predominant causes of King-Denborough Syndrome in an African cohort
www.nature.com
ICGNMD
@icgnmd.bsky.social
· Nov 15