先天性甲状腺功能减退症患儿双氧化酶1基因突变研究
韩文秀,臧红伟,臧玉翠,衣明纪,阎胜利,刘世国,葛银林
Screening of double oxide enzyme mutations in patients with congenital hypothyroidism.
HAN Wen-xiu,ZANG Hong-wei,ZANG Yu-cui,YI Ming-ji,YAN Sheng-li,LIU Shi-guo,GE Yin-lin.
中国儿童保健杂志
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2016, (8): 795
-799
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DOI: 10.11852/zgetbjzz2016-24-08-04
