Eye movement disorders are an early manifestation of CACNA1A mutations in children.
about
Genetic risk factors for glaucoma and exfoliation syndrome identified by genome-wide association studies.Dramatic Response After Lamotrigine in a Patient With Epileptic Encephalopathy and a De NovoCACNA1A Variant.Ocular Manifestation of CACNA1A Pathogenic VariantsStroke-Like Episodes and Cerebellar Syndrome in Phosphomannomutase Deficiency (PMM2-CDG): Evidence for Hypoglycosylation-Driven Channelopathy.
P2860
Eye movement disorders are an early manifestation of CACNA1A mutations in children.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
Eye movement disorders are an early manifestation of CACNA1A mutations in children.
@en
type
label
Eye movement disorders are an early manifestation of CACNA1A mutations in children.
@en
prefLabel
Eye movement disorders are an early manifestation of CACNA1A mutations in children.
@en
P2093
P2860
P356
P1476
Eye movement disorders are an early manifestation of CACNA1A mutations in children.
@en
P2093
Christopher Troedson
Esther M Tantsis
Florence Riant
Lyn Griffiths
Manoj P Menezes
Neven Maksemous
Richard Webster
Robert Ouvrier
Robert Smith
Sachin Gupta
P2860
P304
P356
10.1111/DMCN.13033
P577
2016-01-27T00:00:00Z