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Application of peptide therapy for ligaments and tendons: A narrative review - ScienceDirect
X-linked sideroblastic anemia (XLSA), the most common inherited SA, is caused by a mutation of ALAS2 (for aminolevulinate, delta-, synthase 2), located on chromosome Xp11.21 (144, 145, 146, 147, 148, 149, 150, 151, 152, 153)
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