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A mutation map for human glycoside hydrolase genes

Glycobiology(2020)10.1093/glycob/cwaa010Source: DataRank Database

A mutation map for human glycoside hydrolase genes is a research paper published in Glycobiology (2020). On theSindex it has a DataRank of 0. It has been cited 13 times.

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Open Access13 citations

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Enrichment:Funding (9 grants)OA: bronzeTopics (9)IDs (PubMed, PMC)Annotations (1)

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Findable (1/2)

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Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

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Authors (12)

Diab M. Husein,Birthe Gericke ORCID,Torben Hansen ORCID,Oluf Pedersen ORCID,Mitali A. Tambe ORCID

Live enrichment

PubMed:32039448 PMC:PMC7372926

Danish National Research Foundation

Grant: DNRF107

Lundbeck Foundation

Grant: R223-2016-563

Lundbeck Foundation

Grant: R317-2019-225

National Institutes of Health

Grant: R01 DK099551

NNF Center for Basic Metabolic Research

Grant: Hansen Group

NNF Center for Basic Metabolic Research

Grant: Pedersen Group

Bertrand Might Research Foundation

Lundbeck Foundation Centre for Applied Medical Genomics in Personalized Disease Prediction, Prevention and Care

Læge Sofus Carl Emil Friis og hustru Olga Doris Friis’ Legat

bronzeLicense: https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model

GREENhttps://europepmc.org/articles/pmc7372926?pdf=render

publisherhttps://academic.oup.com/glycob/article-pdf/30/8/500/33646377/cwaa010.pdf

publisherhttp://academic.oup.com/glycob/advance-article-pdf/doi/10.1093/glycob/cwaa010/32870543/cwaa010.pdf

publisherhttp://academic.oup.com/glycob/article-pdf/30/8/500/33646377/cwaa010.pdf

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/7372926

Fields of Study

MedicineBiology

MeSH Terms

HumansGlycoside HydrolasesProteomeMutation

Keywords

WesNssnvCongenital Disorders Of Glycoside Hydrolysis

A mutation map for human glycoside hydrolase genes

FAIR Checklist

Authors (12)

Funding (9 grants)

Open Access

Topics

Annotations (Europe PMC)