Glutaminase Deficiency Caused by Short Tandem Repeat Expansion in
Amino Acid Metabolism, Inborn Errors
/ genetics
Ataxia
/ genetics
Atrophy
/ genetics
Cerebellum
/ pathology
Child, Preschool
Developmental Disabilities
/ genetics
Female
Genotype
Glutaminase
/ deficiency
Glutamine
/ analysis
Humans
Male
Microsatellite Repeats
Mutation
Phenotype
Polymerase Chain Reaction
Whole Genome Sequencing
Journal
The New England journal of medicine
ISSN: 1533-4406
Titre abrégé: N Engl J Med
Pays: United States
ID NLM: 0255562
Informations de publication
Date de publication:
11 04 2019
11 04 2019
Historique:
entrez:
11
4
2019
pubmed:
11
4
2019
medline:
27
4
2019
Statut:
ppublish
Résumé
We report an inborn error of metabolism caused by an expansion of a GCA-repeat tract in the 5' untranslated region of the gene encoding glutaminase (
Identifiants
pubmed: 30970188
doi: 10.1056/NEJMoa1806627
pmc: PMC8819703
mid: NIHMS1529626
doi:
Substances chimiques
Glutamine
0RH81L854J
Glutaminase
EC 3.5.1.2
Types de publication
Case Reports
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1433-1441Subventions
Organisme : Genome Canada
ID : ABC4DE project
Pays : International
Organisme : Intramural NIH HHS
ID : Z01 DK057808-01
Pays : United States
Organisme : Michael Smith Foundation for Health Research
ID : Scholar Award
Pays : International
Organisme : CIHR
ID : 301221
Pays : Canada
Organisme : BC Children's Hospital Foundation
ID : 1st Collaborative Area of Innovation
Pays : International
Organisme : Fondation Brain Canada
ID : Health Canada Platform Support Grant #PSG14-3505
Pays : International
Organisme : CIHR
ID : Rare Diseases Model Organisms and Mechanisms
Pays : Canada
Organisme : Intramural NIH HHS
ID : Z01 DK057808
Pays : United States
Organisme : Natural Sciences and Engineering Research Council of Canada
ID : #05389-14
Pays : International
Commentaires et corrections
Type : CommentIn
Informations de copyright
Copyright © 2019 Massachusetts Medical Society.
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