A familial case of congenital hypothyroidism caused by a homozygous mutation of the thyrotropin receptor gene (Q77205238)
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scientific article published on 01 October 2001
Language | Label | Description | Also known as |
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English | A familial case of congenital hypothyroidism caused by a homozygous mutation of the thyrotropin receptor gene |
scientific article published on 01 October 2001 |
Statements
A familial case of congenital hypothyroidism caused by a homozygous mutation of the thyrotropin receptor gene (English)
Bretones P
Duprez L
Parma J
David M
Vassart G
1 October 2001