id	author	title	date	pages	extension	mime	words	sentences	flesch	summary	cache	txt
work_5qdl2p7kyzdtpg2ztsr3ai5gme	Despina Sanoudou	Clinical and genetic heterogeneity in nemaline myopathy – a disease of skeletal muscle thin filaments	2001.0		.pdf	text/html	1002	203	68	Clinical and genetic heterogeneity in nemaline myopathy--a disease of skeletal muscle thin filaments. Corpus ID: 5825026Clinical and genetic heterogeneity in nemaline myopathy--a disease of skeletal muscle thin filaments. title={Clinical and genetic heterogeneity in nemaline myopathy--a disease of skeletal muscle thin filaments.}, The term nemaline myopathy (NM) encompasses a heterogeneous group of disorders of primary skeletal muscle weakness characterized by the presence of nemaline rods in muscles of affected individuals. Figures, Tables, and Topics from this paper Sort by Most Influenced Papers Sort by Citation Count Heterogeneity of nemaline myopathy cases with skeletal muscle α‐actin gene mutations Clinical and pathological features of patients with nemaline myopathy. Nemaline Myopathy Caused by Mutations in the Muscle α-Skeletal-Actin Gene Nemaline myopathy: comparative muscle histochemistry in the severe neonatal, moderate congenital, and adult-onset forms. Intranuclear rods in severe congenital nemaline myopathy Congenital nemaline myopathy. Semantic Scholar is a free, AI-powered research tool for scientific literature, based at the Allen Institute for AI.	./cache/work_5qdl2p7kyzdtpg2ztsr3ai5gme.pdf	./txt/work_5qdl2p7kyzdtpg2ztsr3ai5gme.txt