It is caused by mutations in the monocarboxylate transporter 8 gene (SLC16A2 [solute carrier family 16, member 2]), located on the X chromosome.
英
美
释义
这是造成基因突变,在单羧酸转运8基因( slc16a2 [溶质载体家族16个,会员2 ] ) ,坐落于x染色体上。
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