CANGÜL, H. Et Al. 2018. Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism.. JCI insight , vol.3, no.20 .

CANGÜL, H., Liao, X., Schoenmakers, E., Kero, J., Barone, S., Srichomkwun, P., ... Iwayama, H.(2018). Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism.. JCI insight , vol.3, no.20.

CANGÜL, HAKAN Et Al. "Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism.," JCI insight , vol.3, no.20, 2018

CANGÜL, HAKAN Et Al. "Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism.." JCI insight , vol.3, no.20, 2018

CANGÜL, H. Et Al. (2018) . "Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism.." JCI insight , vol.3, no.20.

@article{article, author={HAKAN CANGÜL Et Al. }, title={Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism.}, journal={JCI insight}, year=2018}