[[sponsorship]]基因體研究中心[[note]]已出版;[SCI];有審查制度;不具代表性[[note]]http://gateway.isiknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=Drexel&SrcApp=hagerty_opac&KeyRecord=1074-5521&DestApp=JCR&RQ=IF_CAT_BOXPLOT[[note]]http://gateway.isiknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=RID&SrcApp=RID&DestLinkType=FullRecord&DestApp=ALL_WOS&KeyUT=00023379980001
Gaucher disease is an autosomal recessive lysosomal storage disorder caused by the deficient activit...
Gaucher disease is a lysosomal storage disorder characterized by a deficiency of the enzyme acid bet...
We report on a sibship in which three members were affected by Gaucher disease. Molecular analysis o...
SummaryGaucher disease is a lysosomal storage disorder caused by deficient glucocerebrosidase activi...
[[sponsorship]]基因體研究中心[[note]]已出版;[SCI];有審查制度;不具代表性[[note]]http://gateway.isiknowledge.com/gateway/G...
Although Gaucher disease is a rare disorder, recent developments in novel means for therapeutic inte...
Gaucher disease is an autosomal recessive lysosomal disorder characterized by the accumulation of gl...
[Objectives]: Gaucher disease (GD) is the most common inherited lysosomal storage disease, caused by...
[[sponsorship]]基因體研究中心[[note]]已出版;[SCI];有審查制度;不具代表性[[note]]http://gateway.isiknowledge.com/gateway/G...
The molecular diagnosis of Gaucher disease has been difficult due to the existence of several differ...
Type 1 Gaucher disease (GD), the most prevalent lysosomal storage disease, results from the deficien...
Gaucher disease (GD), an autosomal recessive disease, is characterized by accumulation of glucosylce...
Glycosphingolipids (GSLs) are a large and heterogeneous class of lipids, whose function is equally v...
Gaucher disease results from the inherited deficiency of the enzyme glucocerebrosidase (EC 3.2.1.45)...
SummaryGaucher disease (GD) is one of the most prevalent lysosomal storage disorders and one of the ...
Gaucher disease is an autosomal recessive lysosomal storage disorder caused by the deficient activit...
Gaucher disease is a lysosomal storage disorder characterized by a deficiency of the enzyme acid bet...
We report on a sibship in which three members were affected by Gaucher disease. Molecular analysis o...
SummaryGaucher disease is a lysosomal storage disorder caused by deficient glucocerebrosidase activi...
[[sponsorship]]基因體研究中心[[note]]已出版;[SCI];有審查制度;不具代表性[[note]]http://gateway.isiknowledge.com/gateway/G...
Although Gaucher disease is a rare disorder, recent developments in novel means for therapeutic inte...
Gaucher disease is an autosomal recessive lysosomal disorder characterized by the accumulation of gl...
[Objectives]: Gaucher disease (GD) is the most common inherited lysosomal storage disease, caused by...
[[sponsorship]]基因體研究中心[[note]]已出版;[SCI];有審查制度;不具代表性[[note]]http://gateway.isiknowledge.com/gateway/G...
The molecular diagnosis of Gaucher disease has been difficult due to the existence of several differ...
Type 1 Gaucher disease (GD), the most prevalent lysosomal storage disease, results from the deficien...
Gaucher disease (GD), an autosomal recessive disease, is characterized by accumulation of glucosylce...
Glycosphingolipids (GSLs) are a large and heterogeneous class of lipids, whose function is equally v...
Gaucher disease results from the inherited deficiency of the enzyme glucocerebrosidase (EC 3.2.1.45)...
SummaryGaucher disease (GD) is one of the most prevalent lysosomal storage disorders and one of the ...
Gaucher disease is an autosomal recessive lysosomal storage disorder caused by the deficient activit...
Gaucher disease is a lysosomal storage disorder characterized by a deficiency of the enzyme acid bet...
We report on a sibship in which three members were affected by Gaucher disease. Molecular analysis o...