A comprehensive spatiotemporal map of dystrophin isoform expression in the developing and adult human brain
Francesco Catapano(University College London), Francesco Muntoni(National Institute for Health and Care Research)
Cited by 7
Related Papers
Mutations in KLHL40 Are a Frequent Cause of Severe Autosomal-Recessive Nemaline Myopathy
|The American Journal of Human Genetics|2013|224
Identification of KLHL41 Mutations Implicates BTB-Kelch-Mediated Ubiquitination as an Alternate Pathway to Myofibrillar Disruption in Nemaline Myopathy
|The American Journal of Human Genetics|2013|164
Phenotypic and molecular insights into spinal muscular atrophy due to mutations in BICD2
|Brain|2014|100
<scp><i>GGPS1</i></scp>‐associated muscular dystrophy with and without hearing loss
|Annals of Clinical and Translational Neurology|2022|11
A comprehensive spatiotemporal map of dystrophin isoform expression in the developing and adult human brain
|bioRxiv (Cold Spring Harbor Laboratory)|2024|2