A novel mutation in the TG gene (G2322S) causing congenital hypothyroidism in a Sudanese family: a case report.
BMC Med Genet
; 19(1): 69, 2018 05 02.
Article
in En
| MEDLINE
| ID: mdl-29720101
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Thyroglobulin
/
Mutation, Missense
/
Congenital Hypothyroidism
/
Exome Sequencing
Type of study:
Prognostic_studies
Limits:
Female
/
Humans
/
Newborn
Country/Region as subject:
Africa
/
Oceania
Language:
En
Journal:
BMC Med Genet
Journal subject:
GENETICA MEDICA
Year:
2018
Document type:
Article
Affiliation country:
United States
Country of publication:
United kingdom