Old Web
English
Sign In
Acemap
>
Paper
>
Congenital Central Hypothyroidism (CeH) due to a new variant in IGSF1 gene: clinical case of 2 siblings
Congenital Central Hypothyroidism (CeH) due to a new variant in IGSF1 gene: clinical case of 2 siblings
2021
Marco Abbate
Gaia Vincenzi
Marianna R Stancampiano
Biagio Cangiano
Marco Bonomi
Graziano Barera
Maria Cristina Vigone
Keywords:
new variant
Pediatrics
clinical case
Congenital central hypothyroidism
Medicine
IGSF1 gene
Correction
Source
Cite
Save
Machine Reading By IdeaReader
0
References
0
Citations
NaN
KQI
[]