Novel homozygous variant in the TPO gene associated with congenital hypothyroidism and mild-intellectual disability
TPO基因中一种新的纯合变异与先天性甲状腺功能减退症和轻度智力障碍相关
期刊:Human Genome Variation
影响因子:1.3
doi:10.1038/s41439-020-00129-3
Khan, Amjad; Umair, Muhammad; Sharaf, Rania Abdulfattah; Khan, Muhammad Ismail; Ullah, Amir; Abbas, Safdar; Shaheen, Nargis; Bilal, Muhammad; Ahamd, Farooq