C - Chemistry – Metallurgy – 12 – N
Patent
C - Chemistry, Metallurgy
12
N
C12N 15/12 (2006.01) C07K 14/47 (2006.01) C07K 14/705 (2006.01) G01N 33/50 (2006.01) G01N 33/566 (2006.01)
Patent
CA 2347679
The present invention provides methods for identifying abnormalities in human chromosome (11) that are linked to defects in glucose metabolism. The present invention also provides methods for identifying polymorphisms in a new human gene that resides on chromosome 11q23-q24, a locus linked with a heritable form of diabetes.
La présente invention concerne des procédés permettant d'identifier toute anomalie du chromosome humain 11, ces anomalies étant liées à des troubles du métabolisme glucosique. La présente invention concerne également des procédés permettant d'identifier des polymorphismes d'un nouveau gène humain qui réside sur le chromosome 11q23-q24, un site lié à une forme héréditaire de diabète.
Jelinek Laura J.
Sheppard Paul O.
Whitmore Theodore E.
Jelinek Laura J.
Ledgley Law
Sheppard Paul O.
Whitmore Theodore E.
Zymogenetics Inc.
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