Computational biology insights into genotype-clinical phenotype-protein phenotype relationships between novel SLC26A2 variants identified in inherited skeletal dysplasias.
Eur J Med Genet
; 65(10): 104595, 2022 Oct.
Article
in En
| MEDLINE
| ID: mdl-36007841
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Osteochondrodysplasias
/
Computational Biology
Type of study:
Prognostic_studies
/
Qualitative_research
Limits:
Female
/
Humans
/
Pregnancy
Language:
En
Journal:
Eur J Med Genet
Journal subject:
GENETICA MEDICA
Year:
2022
Document type:
Article
Affiliation country:
India