A Novel Rare Missense Variation of the
Adolescent
Adult
Alleles
Child
Crohn Disease
/ genetics
Female
Genetic Association Studies
Genetic Predisposition to Disease
Genotype
Heterozygote
Humans
Immunity, Innate
/ genetics
Male
Mutation
Mutation, Missense
/ genetics
Nod2 Signaling Adaptor Protein
/ chemistry
Peptidoglycan
/ immunology
Polymorphism, Single Nucleotide
Protein Conformation
Exome Sequencing
Crohn’s disease
NOD2 gene
WES
variation
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
15 Feb 2019
15 Feb 2019
Historique:
received:
12
11
2018
revised:
23
01
2019
accepted:
03
02
2019
entrez:
17
2
2019
pubmed:
17
2
2019
medline:
30
5
2019
Statut:
epublish
Résumé
The
Identifiants
pubmed: 30769939
pii: ijms20040835
doi: 10.3390/ijms20040835
pmc: PMC6412783
pii:
doi:
Substances chimiques
NOD2 protein, human
0
Nod2 Signaling Adaptor Protein
0
Peptidoglycan
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Association de l'Etude des Anomalies 174 Congénitales (AEAC)
ID : none
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