Reactome: A Curated Pathway Database
THIS SITE IS USED FOR CURATION AND TESTING
IT IS NOT STABLE, IS LINKED TO AN INCOMPLETE DATA SET, AND IS NOT MONITORED FOR PERFORMANCE. WE STRONGLY RECOMMEND THE USE OF OUR PUBLIC SITE

Query author contributions in Reactome

Reactome depends on collaboration between our curation team and outside experts to assemble and peer-review its pathway modules. The integration of ORCID within Reactome enables us to meet a key challenge with authoring, curating and reviewing biological information by incentivizing and crediting the external experts that contribute their expertise and time to the Reactome curation process. More information is available at ORCID and Reactome.

If you have an ORCID ID that is not listed on this page, please forward this information to us and we will update your Reactome pathway records.

Name Email address

Details on Person Refining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan

Class:IdLiteratureReference:5615545
_displayNameRefining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan
_timestamp2014-07-25 13:31:29
author[Person:5615631] Godfrey, Caroline
[Person:5615599] Clement, Emma
[Person:5615632] Mein, Rachael
[Person:5615546] Brockington, Martin
[Person:5615624] Smith, Janine
[Person:5615627] Talim, Beril
[Person:4084986] Straub, Volker
[Person:5615541] Robb, Stephanie
[Person:5615614] Quinlivan, Ros
[Person:5615551] Feng, Lucy
[Person:5615633] Jimenez-Mallebrera, Cecilia
[Person:4719396] Mercuri, Eugenio
[Person:5615536] Manzur, Adnan Y
[Person:5615584] Kinali, Maria
[Person:5615643] Torelli, Silvia
[Person:5615561] Brown, Susan C
[Person:5615635] Sewry, Caroline A
[Person:4085004] Bushby, Kate
[Person:5615605] Topaloglu, Haluk
[Person:5615615] North, Kathryn
[Person:5615593] Abbs, Stephen
[Person:5615577] Muntoni, Francesco
created[InstanceEdit:5615549] Jassal, Bijay, 2014-07-25
journalBrain
pages2725-35
pubMedIdentifier17878207
titleRefining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan
volume130
year2007
(literatureReference)[FailedReaction:5615556] Defective POMT2 does not transfer Man from Dol-P-Man to DAG1 [Homo sapiens]
[FailedReaction:5615604] Defective POMT1 does not transfer Man from Dol-P-Man to DAG1 [Homo sapiens]
[FailedReaction:5617096] Defective POMGNT1 does not transfer GlcNAc from UDP-GlcNAc to Man-O-Ser-DAG1 [Homo sapiens]
[Change default viewing format]
No pathways have been reviewed or authored by Refining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan (5615545)