A homozygous mutation in the highly conserved Tyr60 of the mature IGF1 peptide broadens the spectrum of IGF1 deficiency.
Eur J Endocrinol
; 181(5): K43-K53, 2019 Nov.
Article
in En
| MEDLINE
| ID: mdl-31539878
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Insulin-Like Growth Factor I
/
Mutation, Missense
/
Growth Disorders
/
Hearing Loss, Sensorineural
Type of study:
Prognostic_studies
Limits:
Humans
/
Infant
/
Male
Language:
En
Journal:
Eur J Endocrinol
Journal subject:
ENDOCRINOLOGIA
Year:
2019
Type:
Article
Affiliation country:
Argentina