TUBB4A mutations result in specific neuronal and oligodendrocytic defects that closely match clinically distinct phenotypes.
Hum Mol Genet
; 26(22): 4506-4518, 2017 11 15.
Article
in En
| MEDLINE
| ID: mdl-28973395
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Tubulin
/
Oligodendroglia
/
Neurons
Language:
En
Journal:
Hum Mol Genet
Journal subject:
BIOLOGIA MOLECULAR
/
GENETICA MEDICA
Year:
2017
Type:
Article
Affiliation country:
United States