[A study of 2 congenital hypothyroid goiters in siblings: identification of a genetic abnormality in thyroid hormonogenesis marked by the absence of thyroglobulin and by the iodination of unsuitable proteins rich in iodohistidine and deficient in thyroxine].
作者信息
Savoie J C, Massin J P, Sizonenko P C, Job J C
出版信息
Ann Endocrinol (Paris). 1973 Sep-Oct;34(5):539-48.
PMID:4136284
Abstract
摘要
Zotero 插件