Natural history and genetic study of LAMA2-related muscular dystrophy in a large Chinese cohort

Overview of attention for article published in Orphanet Journal of Rare Diseases, July 2021

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RT @kgmr_rad: LAMA2関連筋ジストロフィー＝メロシン欠損型先天性筋ジストロフィー欧米では非福山型の約半数はメロシン欠損型、本邦は稀知的障害を伴わない先天性筋ジストロフィー CK↑白質病変(脳梁、内包は保たれる) https://t.co/9Je0OkGSEZ

Natural history and genetic study of LAMA2-related muscular dystrophy in a large Chinese cohort https://t.co/5yopVFFjdm

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