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FLJ42485
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The clinical spectrum of the congenital myasthenic syndrome resulting from COL13A1 mutations.
Myasthenic syndromes due to defects in COL13A1 and in the N-linked glycosylation pathway.
TGF-β2 and collagen play pivotal roles in the spheroid formation and anti-aging of human dermal papi…
Moderate phenotype of a congenital myasthenic syndrome type 19 caused by mutation of the COL13A1 gen…
Downregulation of COL12A1 and COL13A1 by a selective EP2 receptor agonist, omidenepag, in human trab…
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