Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism

Approved

Classifications

MinEdu publication type
A1
Category
Artikkelit ja abstraktit
Refereed
Kyllä
Sub category
Tieteelliset aikakauslehtiartikkelit
Type
Alkuperäisartikkeli

Authors of the publication

Number of authors
27
Authors
Cangul, H; Liao, XH; Schoenmakers, E; Kero, J; Barone, S; Srichomkwun, P; Iwayama, H; Serra, EG; Saglam, H; Eren, E; Tarim, O; Nicholas, AK; Zvetkova, I; Anderson, CA; Frankl, FE; Boelaert, K; Ojaniemi, M; Jääskeläinen, J; Patyra, K; Löf, C; et al

Publication channel information

Title of journal/series
JCI insight
ISSN (electronic)
2379-3708
ISSN (linking)
2379-3708
Publication forum ID
85116
Publication forum level
1
Internationality
Yes

Detailed publication information

Publication year
2018
Reporting year
2018
Journal/series volume number
3
Journal/series issue number
20
Page numbers
e99631
DOI
10.1172/jci.insight.99631
Language of publication
English

Co-publication information

International co-publication
Yes
Co-publication with a company
No

Availability

Link to self-archived version
https://erepo.uef.fi/handle/123456789/7082

Classification and additional information

MinEdu field of science classification
3121 General medicine, internal medicine and other clinical medicine, 1184 Genetics, developmental biology, physiology