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[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

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