10:45 AM - 10:55 AM
[O5-1] Function study of NKX2-1 gene c.799G>T mutation, which caused congenital hypothyroidism and central nervous system disorders
The password will be announced in the abstract book.
APPES/JSPE Joint Session(English)
APPES/JSPE Joint Session(English) » Oral
Sat. Nov 19, 2016 10:45 AM - 11:45 AM Room 2 (Hall B7 (1))
Moderator: Kanshi Minamitani (Department of Pediatrics, Teikyo University Chiba Medical Center), Nalini S. Shah (Department of Endocrinology, Seth G S Medical College & KEM Hospital Mumbai)
10:45 AM - 10:55 AM
The password will be announced in the abstract book.