(Q28304128)

object named as

G M Lathrop

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author name string

M Vaxillaire

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V Boccio

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C Vigouroux

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J Terwilliger

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P Passa

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J S Beckmann

Close linkage of glucokinase locus on chromosome 7p to early-onset non-insulin-dependent diabetes mellitus

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language of work or name

English

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publication date

April 1995

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418-23

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cites work

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-418

Familial hyperglycemia due to mutations in glucokinase. Definition of a subtype of diabetes mellitus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-418

A second-generation linkage map of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-418

Primary pancreatic beta-cell secretory defect caused by mutations in glucokinase gene in kindreds of maturity onset diabetes of the young

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-418

Scope and heterogeneous nature of MODY.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-418

7 January 2021

Strategies for the collection of sibling-pair data for genetic studies in type 2 (non-insulin-dependent) diabetes mellitus

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-418

7 January 2021

Gene for non-insulin-dependent diabetes mellitus (maturity-onset diabetes of the young subtype) is linked to DNA polymorphism on human chromosome 20q

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-418

7 January 2021

Glucokinase mutations associated with non-insulin-dependent (type 2) diabetes mellitus have decreased enzymatic activity: implications for structure/function relationships

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-418

7 January 2021

Search for a third susceptibility gene for maturity-onset diabetes of the young. Studies with eleven candidate genes

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-418

7 January 2021

Abnormal insulin secretion, not insulin resistance, is the genetic or primary defect of MODY in the RW pedigree.

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-418

7 January 2021