alg9 gene
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Identification and Functional Analysis of a Defect in the Human ALG9 Gene: Definition of Congenital Disorder of Glycosylation Type IL

The American Journal of Human Genetics ◽

10.1086/422367 ◽

2004 ◽

Vol 75 (1) ◽

pp. 146-150 ◽

Cited By ~ 60

Author(s):

Christian G. Frank ◽

Wafaa Eyaid ◽

Eric G. Berger ◽

Markus Aebi ◽

Claudia E. Grubenmann ◽

...

Keyword(s):

Functional Analysis ◽

Congenital Disorder ◽

Congenital Disorder Of Glycosylation ◽

Gene Definition ◽

Definition Of ◽

Alg9 Gene

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Stepwise assembly of the lipid-linked oligosaccharide in the endoplasmic reticulum of Saccharomyces cerevisiae: identification of the ALG9 gene encoding a putative mannosyl transferase.

Proceedings of the National Academy of Sciences ◽

10.1073/pnas.93.14.7160 ◽

1996 ◽

Vol 93 (14) ◽

pp. 7160-7165 ◽

Cited By ~ 62

Author(s):

P. Burda ◽

S. te Heesen ◽

A. Brachat ◽

A. Wach ◽

A. Dusterhoft ◽

...

Keyword(s):

Saccharomyces Cerevisiae ◽

Endoplasmic Reticulum ◽

Gene Encoding ◽

Stepwise Assembly ◽

Alg9 Gene ◽

Mannosyl Transferase

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