BVVL/ FL: features caused by SLC52A3 mutations; WDFY4 and TNFSF13B may be novel causative genes.
Neurobiol Aging
; 99: 102.e1-102.e10, 2021 03.
Article
in En
| MEDLINE
| ID: mdl-33189404
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Bulbar Palsy, Progressive
/
Membrane Transport Proteins
/
Intracellular Signaling Peptides and Proteins
/
B-Cell Activating Factor
/
Genetic Association Studies
/
Mutation
Type of study:
Diagnostic_studies
/
Prognostic_studies
/
Risk_factors_studies
Limits:
Female
/
Humans
/
Male
Language:
En
Journal:
Neurobiol Aging
Year:
2021
Document type:
Article
Affiliation country:
Iran
Country of publication:
United States