Lysosomes and the pathogenesis of merosin-deficient congenital muscular dystrophy.
Sign Up to like & getrecommendations! Published in 2021 at "Human molecular genetics"
DOI: 10.1093/hmg/ddab278
Abstract: Congenital muscular dystrophy type 1A (MDC1A), the most common congenital muscular dystrophy in Western countries, is caused by recessive mutations in LAMA2, the gene encoding laminin alpha 2. Currently, no cure or disease modifying therapy… read more here.
Keywords: lysosomes pathogenesis; caf zebrafish; pathogenesis merosin; congenital muscular ... See more keywords