Congenital Secondary Hypothyroidism Caused by Exon Skipping due to a Homozygous Donor Splice Site Mutation in the TSHβ-Subunit Gene (Q34109180)
scientific article published on January 1, 2002
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(P31) (Q13442814)
(P50) (Q29349874)
(P304) 336-339
(P407) (Q1860)
(P433) 1
(P478) 87
(P577) Tuesday, January 1, 2002
Tuesday, January 1, 2002
(P921) (Q727096)
(Q114049690)
(Q531012)
(P953) https://academic.oup.com/jcem/article-pdf/87/1/336/9158345/jcem0336.pdf
http://academic.oup.com/jcem/article-pdf/87/1/336/9158345/jcem0336.pdf
(P1433) (Q3186902)
(P1476) "Congenital secondary hypothyroidism caused by exon skipping due to a homozygous donor splice site mutation in the TSHbeta-subunit gene" (language: en)
"Congenital Secondary Hypothyroidism Caused by Exon Skipping due to a Homozygous Donor Splice Site Mutation in the TSHβ-Subunit Gene" (language: en)
(P2093) Joachim Pohlenz
Alexandra Dumitrescu
Ulrich Aumann
Gerhard Koch
Ralph Melchior
Dirk Prawitt
(P2860) (Q69666233)
(Q78125348)
(Q46310731)
(Q37352572)
(Q73963652)
(Q42829232)
(Q40906745)
(Q74108602)
other details
description scientific article published on January 1, 2002

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