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pro vyhledávání: '"Ruolin Ren"'
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Limb-girdle muscular dystrophy type 2A (LGMD R1 Calpain 3-Related, LGMD2A/R1), an autosomal recessive disorder, is characterized by progressive muscle weakness with a prominent presentation in the proximal limb girdle muscles. LGMD2A/R1, which is cau
Externí odkaz:
https://doaj.org/article/45100f3e2cd3440fae425f954f405519
Publikováno v:
Modern Food Science & Technology; 2022, Vol. 38 Issue 6, p74-83, 10p
Autor:
The Washington Post
Publikováno v:
Washington Post, The. 08/19/2016.