An identical DCTN1 mutation in two Chinese siblings manifest as dHMN and ALS respectively: a case report.
Amyotroph Lateral Scler Frontotemporal Degener
; 23(1-2): 149-153, 2022 02.
Article
in En
| MEDLINE
| ID: mdl-34615428
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Amyotrophic Lateral Sclerosis
Type of study:
Diagnostic_studies
/
Prognostic_studies
Limits:
Humans
Country/Region as subject:
Asia
Language:
En
Journal:
Amyotroph Lateral Scler Frontotemporal Degener
Year:
2022
Document type:
Article
Country of publication:
United kingdom