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Homozygous DUOXA2 mutation (p.Tyr138*) in a girl with conge..:
Sugisawa, Chiho
;
Higuchi, Shinji
;
Takagi, Masaki
...
Endocrine Journal. 64 (2017) 8 - p. 807-812 , 2017
Link:
https://doi.org/10.1507/endocrj.ej16-0564
RT Journal T1
Homozygous DUOXA2 mutation (p.Tyr138*) in a girl with congenital hypothyroidism and her apparently unaffected brother: Case report and review of the literature
UL https://suche.suub.uni-bremen.de/peid=cr-10.1507_endocrj.ej16-0564&Exemplar=1&LAN=DE A1 Sugisawa, Chiho A1 Higuchi, Shinji A1 Takagi, Masaki A1 Hasegawa, Yukihiro A1 Taniyama, Matsuo A1 Abe, Kiyomi A1 Hasegawa, Tomonobu A1 Narumi, Satoshi PB Japan Endocrine Society YR 2017 SN 0918-8959 SN 1348-4540 JF Endocrine Journal VO 64 IS 8 SP 807 OP 812 LK http://dx.doi.org/https://doi.org/10.1507/endocrj.ej16-0564 DO https://doi.org/10.1507/endocrj.ej16-0564 SF ELIB - SuUB Bremen
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