Novel heterozygous c.798C>G and c.1040T>G mutations in the GBA1 gene are associated with a severe phenotype of Gaucher disease type 1.
about
Novel heterozygous c.798C>G and c.1040T>G mutations in the GBA1 gene are associated with a severe phenotype of Gaucher disease type 1.
description
2014 nî lūn-bûn
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2014年の論文
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2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
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2014年论文
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2014年论文
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name
Novel heterozygous c.798C>G an ...... ype of Gaucher disease type 1.
@en
Novel heterozygous c.798C>G an ...... ype of Gaucher disease type 1.
@nl
type
label
Novel heterozygous c.798C>G an ...... ype of Gaucher disease type 1.
@en
Novel heterozygous c.798C>G an ...... ype of Gaucher disease type 1.
@nl
prefLabel
Novel heterozygous c.798C>G an ...... ype of Gaucher disease type 1.
@en
Novel heterozygous c.798C>G an ...... ype of Gaucher disease type 1.
@nl
P2860
P1433
P1476
Novel heterozygous c.798C>G an ...... type of Gaucher disease type 1
@en
P2093
Maciej Machaczka
Monika Klimkowska
P2860
P304
P356
10.1007/S00277-014-2036-X
P577
2014-02-28T00:00:00Z