It is caused by mutations in the monocarboxylate transporter 8 gene (SLC16A2 [solute carrier family 16, member 2]), located on the X chromosome.

 
  • 這是造成基因突變,在單羧酸轉運8基因( slc16a2 [溶質(zhì)載體家族16個(gè),會(huì )員2 ] ) ,坐落于x染色體上。
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