Thyroid dyshormonogenesis is mainly caused by TPO mutations in consanguineous community

Clinical Endocrinology

Volumn 79, Issue 2, 2013, Pages 275-281

  Cangul, Hakan ^a,b   Aycan, Zehra ^c   Olivera Nappa, Alvaro ^d   Saglam, Halil ^e   Schoenmakers, Nadia A ^d   Boelaert, Kristien ^b   Cetinkaya, Semra ^c   Tarim, Omer ^e   Bober, Ece ^f   Darendeliler, Feyza ^g   Bas, Veysel ^c   Demir, Korcan ^f   Aydin, Banu K ^g   Kendall, Michaela ^h   Cole, Trevor ⁱ   Högler, Wolfgang ^j   Chatterjee, V Krishna K ^d   Barrett, Timothy G ^c   Maher, Eamonn R ^c  

^a BAHCESEHIR UNIVERSITY   (Turkey)

^b UNIVERSITY OF BIRMINGHAM   (United Kingdom)

^c Social Security Institution   (Turkey)

^d UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^e ULUDAG UNIVERSITY   (Turkey)

^f DOKUZ EYLUL UNIVERSITY   (Turkey)

^g ISTANBUL UNIVERSITY   (Turkey)

^h UNIVERSITY OF SOUTHAMPTON   (United Kingdom)

ⁱ BIRMINGHAM WOMEN S HOSPITAL   (United Kingdom)

^j BIRMINGHAM CHILDREN S HOSPITAL   (United Kingdom)

more..

Author keywords

[No Author keywords available]

Indexed keywords

DIIODOTYROSINE; LEVOTHYROXINE; PENDRIN; SODIUM IODIDE SYMPORTER; THYROGLOBULIN; THYROID PEROXIDASE;

ADULT; ARTICLE; CHILD; CLINICAL CLASSIFICATION; CONGENITAL HYPOTHYROIDISM; ENDOCRINE DISEASE; FEMALE; GENOTYPE PHENOTYPE CORRELATION; HUMAN; HYROID DYSHORMONOGENESIS; LINKAGE ANALYSIS; MAJOR CLINICAL STUDY; MALE; MISSENSE MUTATION; PRESCHOOL CHILD; PRIORITY JOURNAL; THYROID HORMONE SYNTHESIS;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; CONGENITAL HYPOTHYROIDISM; CONSANGUINITY; FEMALE; HUMANS; INFANT; INFANT, NEWBORN; IODIDE PEROXIDASE; MALE; MUTATION, MISSENSE; PAKISTAN; THYROID HORMONES; TURKEY;

EID: 84880072335     PISSN: 03000664     EISSN: 13652265     Source Type: Journal    
DOI: 10.1111/cen.12127     Document Type: Article

References (13)

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