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 G. Serra
Halil Saglam
Erdal Eren
Omer 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:
Congenital hypothyroidism
Loss function
Pediatrics
Medicine
Correction
Source
Cite
Save
Machine Reading By IdeaReader
0
References
0
Citations
NaN
KQI
[]