The c.859G>C variant in the SMN2 gene is associated with types II and III SMA and originates from a common ancestor.
J Med Genet
; 47(9): 640-2, 2010 Sep.
Article
in En
| MEDLINE
| ID: mdl-20577007
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Phylogeny
/
Muscular Atrophy, Spinal
/
Survival of Motor Neuron 2 Protein
/
Mutation
Type of study:
Risk_factors_studies
Limits:
Adolescent
/
Child
/
Child, preschool
/
Female
/
Humans
/
Male
Country/Region as subject:
Europa
Language:
En
Journal:
J Med Genet
Year:
2010
Document type:
Article