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Genotype-phenotype correlation of biallelic DUOX2 mutations in transient and permanent congenital hypothyroidism.

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Title: Genotype-phenotype correlation of biallelic DUOX2 mutations in transient and permanent congenital hypothyroidism.
Authors: Liang SB; Department of Pediatrics, Taipei Veterans General Hospital, Taipei 11217, Taiwan., Cheng CY; Department of Pediatrics, Taipei Veterans General Hospital, Taipei 11217, Taiwan., Chen YR; Department of Pediatrics, Taipei Veterans General Hospital, Taipei 11217, Taiwan., Chen YJ; Department of Pediatrics, Taipei Veterans General Hospital, Taipei 11217, Taiwan.; Department of Life Sciences and Institute of Genome Sciences, National Yang Ming Chiao Tung University, Taipei 112304, Taiwan., Yang CF; Department of Pediatrics, Taipei Veterans General Hospital, Taipei 11217, Taiwan.; School of Medicine, National Yang Ming Chiao Tung University, Taipei 112304, Taiwan., Lu YH; Department of Pediatrics, Taipei Veterans General Hospital, Taipei 11217, Taiwan., Niu DM; Department of Pediatrics, Taipei Veterans General Hospital, Taipei 11217, Taiwan.; Institute of Clinical Medicine, School of Medicine, National Yang Ming Chiao Tung University, Taipei 112304, Taiwan.; Institute of Molecular and Genomic Medicine, National Health Research Institutes, Miaoli 35053, Taiwan.
Source: Journal of the Endocrine Society [J Endocr Soc] 2026 Apr 13; Vol. 10 (6), pp. bvag081. Date of Electronic Publication: 2026 Apr 13 (Print Publication: 2026).
Publication Type: Journal Article
Journal Info: Publisher: Endocrine Society Country of Publication: United States NLM ID: 101697997 Publication Model: eCollection Cited Medium: Internet ISSN: 2472-1972 (Electronic) Linking ISSN: 24721972 NLM ISO Abbreviation: J Endocr Soc Subsets: PubMed not MEDLINE
Database: MEDLINE Ultimate
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  Data: Genotype-phenotype correlation of biallelic DUOX2 mutations in transient and permanent congenital hypothyroidism.
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  Data: <searchLink fieldCode="AU" term="%22Liang+SB%22">Liang SB</searchLink>; Department of Pediatrics, Taipei Veterans General Hospital, Taipei 11217, Taiwan.<br /><searchLink fieldCode="AU" term="%22Cheng+CY%22">Cheng CY</searchLink>; Department of Pediatrics, Taipei Veterans General Hospital, Taipei 11217, Taiwan.<br /><searchLink fieldCode="AU" term="%22Chen+YR%22">Chen YR</searchLink>; Department of Pediatrics, Taipei Veterans General Hospital, Taipei 11217, Taiwan.<br /><searchLink fieldCode="AU" term="%22Chen+YJ%22">Chen YJ</searchLink>; Department of Pediatrics, Taipei Veterans General Hospital, Taipei 11217, Taiwan.; Department of Life Sciences and Institute of Genome Sciences, National Yang Ming Chiao Tung University, Taipei 112304, Taiwan.<br /><searchLink fieldCode="AU" term="%22Yang+CF%22">Yang CF</searchLink>; Department of Pediatrics, Taipei Veterans General Hospital, Taipei 11217, Taiwan.; School of Medicine, National Yang Ming Chiao Tung University, Taipei 112304, Taiwan.<br /><searchLink fieldCode="AU" term="%22Lu+YH%22">Lu YH</searchLink>; Department of Pediatrics, Taipei Veterans General Hospital, Taipei 11217, Taiwan.<br /><searchLink fieldCode="AU" term="%22Niu+DM%22">Niu DM</searchLink>; Department of Pediatrics, Taipei Veterans General Hospital, Taipei 11217, Taiwan.; Institute of Clinical Medicine, School of Medicine, National Yang Ming Chiao Tung University, Taipei 112304, Taiwan.; Institute of Molecular and Genomic Medicine, National Health Research Institutes, Miaoli 35053, Taiwan.
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  Data: <searchLink fieldCode="JN" term="%22101697997%22">Journal of the Endocrine Society</searchLink> [J Endocr Soc] 2026 Apr 13; Vol. 10 (6), pp. bvag081. <i>Date of Electronic Publication: </i>2026 Apr 13 (<i>Print Publication: </i>2026).
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Endocrine+Society%22">Endocrine Society </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>101697997 <i>Publication Model: </i>eCollection <i>Cited Medium: </i>Internet <i>ISSN: </i>2472-1972 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2224721972%22">24721972 </searchLink><i>NLM ISO Abbreviation: </i>J Endocr Soc <i>Subsets: </i>PubMed not MEDLINE
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      – Type: doi
        Value: 10.1210/jendso/bvag081
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      – Code: eng
        Text: English
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        StartPage: bvag081
    Titles:
      – TitleFull: Genotype-phenotype correlation of biallelic DUOX2 mutations in transient and permanent congenital hypothyroidism.
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            NameFull: Liang SB
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            NameFull: Cheng CY
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            – D: 13
              M: 04
              Text: 2026 Apr 13
              Type: published
              Y: 2026
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              Value: 2472-1972
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              Value: 10
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              Value: 6
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