Co-existence of lysosomal storage diseases in a consanguineous family.
about
Quantification of homozygosity in consanguineous individuals with autosomal recessive disease.Aspartylglucosaminuria: unusual neonatal presentation in Qatari twins with a novel aspartylglucosaminidase gene mutation and 3 new cases in a Turkish family.Disability in children from different ethnic populations.Mutation identification of Fabry disease in families with other lysosomal storage disorders.
P2860
Co-existence of lysosomal storage diseases in a consanguineous family.
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年学术文章
@wuu
2001年学术文章
@zh
2001年学术文章
@zh-cn
2001年学术文章
@zh-hans
2001年学术文章
@zh-my
2001年学术文章
@zh-sg
2001年學術文章
@yue
2001年學術文章
@zh-hant
name
Co-existence of lysosomal storage diseases in a consanguineous family.
@en
Co-existence of lysosomal storage diseases in a consanguineous family.
@nl
type
label
Co-existence of lysosomal storage diseases in a consanguineous family.
@en
Co-existence of lysosomal storage diseases in a consanguineous family.
@nl
prefLabel
Co-existence of lysosomal storage diseases in a consanguineous family.
@en
Co-existence of lysosomal storage diseases in a consanguineous family.
@nl
P2093
P2860
P1476
Co-existence of lysosomal storage diseases in a consanguineous family.
@en
P2093
P2860
P304
P356
10.1046/J.1365-2214.2001.00165.X
P407
P577
2001-03-01T00:00:00Z