Sandhoff disease: a prevalent form of infantile GM2 gangliosidosis in Lebanon
about
Structure and distribution of an Alu-type deletion mutation in Sandhoff diseaseNatural history of infantile G(M2) gangliosidosis.GM2-Gangliosidosis (Sandhoff and Tay Sachs disease): Diagnosis and Neuroimaging Findings (An Iranian Pediatric Case Series).Sandhoff disease heterozygote detection: a component of population screening for Tay-Sachs disease carriers. II. Sandhoff disease gene frequencies in American Jewish and non-Jewish populations.Five related Lebanese individuals with high plasma lysosomal hydrolases: a new defect in mannose-6-phosphate receptor recognition?Sandhoff disease heterozygote detection: a component of population screening for Tay-Sachs disease carriers. I. Statistical methods.Spectrum of paediatric lysosomal storage disorders in oman.
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P2860
Sandhoff disease: a prevalent form of infantile GM2 gangliosidosis in Lebanon
description
1981 nî lūn-bûn
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1981 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1981 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1981年の論文
@ja
1981年論文
@yue
1981年論文
@zh-hant
1981年論文
@zh-hk
1981年論文
@zh-mo
1981年論文
@zh-tw
1981年论文
@wuu
name
Sandhoff disease: a prevalent form of infantile GM2 gangliosidosis in Lebanon
@ast
Sandhoff disease: a prevalent form of infantile GM2 gangliosidosis in Lebanon
@en
type
label
Sandhoff disease: a prevalent form of infantile GM2 gangliosidosis in Lebanon
@ast
Sandhoff disease: a prevalent form of infantile GM2 gangliosidosis in Lebanon
@en
prefLabel
Sandhoff disease: a prevalent form of infantile GM2 gangliosidosis in Lebanon
@ast
Sandhoff disease: a prevalent form of infantile GM2 gangliosidosis in Lebanon
@en
P2093
P2860
P1476
Sandhoff disease: a prevalent form of infantile GM2 gangliosidosis in Lebanon
@en
P2093
Der Kaloustian VM
P2860
P407
P577
1981-01-01T00:00:00Z