Spinocerebellar Ataxia 21 with Retardation
Investigators at Universite de Lille Nord de France, and other centers in France, report the identification of a novel causative gene for spinocerebellar ataxia 21, an autosomal dominant disorder, initially mapped to chromosome 7 and designated as SCA21.
Saved in:
| Main Authors: | J Gordon Millichap, John J Millichap |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Pediatric Neurology Briefs Publishers
2014-11-01
|
| Series: | Pediatric Neurology Briefs |
| Subjects: | |
| Online Access: | https://www.pediatricneurologybriefs.com/articles/68 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Effects of Topiramate on Language Functions
by: J Gordon Millichap, et al.
Published: (2014-11-01) -
Manifestations of Ictal Fear
by: J Gordon Millichap, et al.
Published: (2014-11-01) -
Cognitive Outcome of Childhood-Onset Multiple Sclerosis Patients
by: J Gordon Millichap, et al.
Published: (2014-11-01) -
Fetal Alcohol Spectrum Disorder Prevalence
by: J Gordon Millichap, et al.
Published: (2014-12-01) -
Tuberous Sclerosis Complex and Arachnoid Cysts
by: J Gordon Millichap, et al.
Published: (2014-12-01)