A mutation in the human ortholog of the Saccharomyces cerevisiae ALG6 gene causes carbohydrate-deficient glycoprotein syndrome type-Ic

Proceedings of the National Academy of Sciences of the United States of America

Volumn 96, Issue 12, 1999, Pages 6982-6987

  Imbach, Timo ^a   Burda, Patricie ^b   Kuhnert, Peter ^c   Wevers, Ron A ^d   Aebi, Markus ^b   Berger, Eric G ^a   Hennet, Thierry ^a  

^a UNIVERSITY OF ZURICH   (Switzerland)

^b ETH ZURICH   (Switzerland)

^c UNIVERSITY OF BERN   (Switzerland)

^d RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CONGENITAL DISORDER OF GLYCOSYLATION; CONTROLLED STUDY; ENDOPLASMIC RETICULUM; GENE MUTATION; HUMAN; HUMAN CELL; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SACCHAROMYCES CEREVISIAE;

AMINO ACID SEQUENCE; BASE SEQUENCE; CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME; DNA, COMPLEMENTARY; GLUCOSYLTRANSFERASES; HUMANS; MEMBRANE PROTEINS; MOLECULAR SEQUENCE DATA; MUTATION; SACCHAROMYCES CEREVISIAE; SEQUENCE ALIGNMENT; SEQUENCE ANALYSIS;

FUNGI; MYXOGASTRIA; SACCHAROMYCES CEREVISIAE;

EID: 0033536073     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.96.12.6982     Document Type: Article

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