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Sandhoff Disease without Hepatosplenomegaly Due to Hexosaminidase B Gene Mutation.GM2-Gangliosidosis (Sandhoff and Tay Sachs disease): Diagnosis and Neuroimaging Findings (An Iranian Pediatric Case Series).Clinical presentation and outcome in infantile Sandhoff disease: a case series of 25 patients from Iranian neurometabolic bioregistry with five novel mutations
P2860
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年学术文章
@wuu
1997年学术文章
@zh-cn
1997年学术文章
@zh-hans
1997年学术文章
@zh-my
1997年学术文章
@zh-sg
1997年學術文章
@yue
1997年學術文章
@zh
1997年學術文章
@zh-hant
name
Sandhoff disease in the Turkish population.
@en
Sandhoff disease in the Turkish population.
@nl
type
label
Sandhoff disease in the Turkish population.
@en
Sandhoff disease in the Turkish population.
@nl
prefLabel
Sandhoff disease in the Turkish population.
@en
Sandhoff disease in the Turkish population.
@nl
P2093
P1476
Sandhoff disease in the Turkish population.
@en
P2093
P304
P356
10.1016/S0387-7604(97)00061-2
P577
1997-11-01T00:00:00Z