Old Web
English
Sign In
Acemap
>
Paper
>
Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism
Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism
2019
Hakan Cangul
Xiao-hui Liao
Erik Schoenmakers
Jukka Kero
Sharon Barone
Panudda Srichomkwun
Hideyuki Iwayama
Eva Serra
Halil Sağlam
Erdal Eren
Ömer Tarim
Adeline K Nicholas
Zvetkova I
Carl A. Anderson
Frankl Fek
Kristien Boelaert
Marja Ojaniemi
Jarmo Jääskeläinen
Konrad Patyra
Christoffer Löf
Williams Ed
Manoocher Soleimani
Timothy Barrett
Eamonn R. Maher
V K K Chatterjee
Samuel Refetoff
Nadia Schoenmakers
Keywords:
Pediatrics
Loss function
Medicine
Congenital hypothyroidism
Correction
Cite
Save
Machine Reading By IdeaReader
0
References
0
Citations
NaN
KQI
[]