A novel mutation in TTC19 associated with isolated complex III deficiency, cerebellar hypoplasia, and bilateral basal ganglia lesions.
about
A novel mutation in TTC19 associated with isolated complex III deficiency, cerebellar hypoplasia, and bilateral basal ganglia lesions.
description
2014 nî lūn-bûn
@nan
2014 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
A novel mutation in TTC19 asso ...... lateral basal ganglia lesions.
@ast
A novel mutation in TTC19 asso ...... lateral basal ganglia lesions.
@en
A novel mutation in TTC19 asso ...... lateral basal ganglia lesions.
@nl
type
label
A novel mutation in TTC19 asso ...... lateral basal ganglia lesions.
@ast
A novel mutation in TTC19 asso ...... lateral basal ganglia lesions.
@en
A novel mutation in TTC19 asso ...... lateral basal ganglia lesions.
@nl
prefLabel
A novel mutation in TTC19 asso ...... lateral basal ganglia lesions.
@ast
A novel mutation in TTC19 asso ...... lateral basal ganglia lesions.
@en
A novel mutation in TTC19 asso ...... lateral basal ganglia lesions.
@nl
P2093
P2860
P356
P1476
A novel mutation in TTC19 asso ...... ilateral basal ganglia lesions
@en
P2093
Alice Zanolini
Bassam Y Abu Libdeh
Laura Melchionda
Nadirah S Damseh
Orly Elpeleg
P2860
P356
10.3389/FGENE.2014.00397
P577
2014-11-14T00:00:00Z