Complicated hereditary spastic paraparesis with cerebral white matter lesions.
about
X-linked spastic paraplegia (SPG1), MASA syndrome and X-linked hydrocephalus result from mutations in the L1 geneX-linked sideroblastic anemia and ataxia: linkage to phosphoglycerate kinase at Xq13.Clinical features of affected males with X linked ocular albinism.Association of late onset spastic paraparesis and dementia: probably an autosomal dominant form of complicated paraplegia.Further evidence for a fourth gene causing X-linked pure spastic paraplegia.Brain atrophy in pure and complicated hereditary spastic paraparesis: a quantitative 3D MRI study.
P2860
Complicated hereditary spastic paraparesis with cerebral white matter lesions.
description
1990 nî lūn-bûn
@nan
1990年の論文
@ja
1990年論文
@yue
1990年論文
@zh-hant
1990年論文
@zh-hk
1990年論文
@zh-mo
1990年論文
@zh-tw
1990年论文
@wuu
1990年论文
@zh
1990年论文
@zh-cn
name
Complicated hereditary spastic paraparesis with cerebral white matter lesions.
@en
Complicated hereditary spastic paraparesis with cerebral white matter lesions.
@nl
type
label
Complicated hereditary spastic paraparesis with cerebral white matter lesions.
@en
Complicated hereditary spastic paraparesis with cerebral white matter lesions.
@nl
prefLabel
Complicated hereditary spastic paraparesis with cerebral white matter lesions.
@en
Complicated hereditary spastic paraparesis with cerebral white matter lesions.
@nl
P2093
P2860
P356
P1476
Complicated hereditary spastic paraparesis with cerebral white matter lesions.
@en
P2093
Fischbeck KH
Gutmann DH
P2860
P304
P356
10.1002/AJMG.1320360222
P577
1990-06-01T00:00:00Z