[文献资料]【参考文献】

1 ． Fricke‐Ottos，Pfarr N，Muhlenberg R，et al ． Mild congenital primary hypothyroidism in a Turkish family caused by a homozygous missense thyrotropin receptor（TSHR）gene mutation（A593V）． Exp Clin Endo crinol Diabetes，2005，113.4 ． Hager‐Malecka B，Sliwa F，Jan ......