A novel TGM1 mutation, leading to multiple splicing rearrangements, is associated with autosomal recessive congenital ichthyosis
Summary Autosomal recessive congenital ichthyosis (ARCI) is a group of rare, clinically heterogeneous skin disorders that affect cornification. ARCI includes lamellar ichthyosis, congenital ichthyosiform erythroderma and harlequin ichthyosis. TGM1 mutations cause > 50% of ARCI cases in the USA. W...
- Autores:
- Tipo de recurso:
- Fecha de publicación:
- 2015
- Institución:
- Universidad del Rosario
- Repositorio:
- Repositorio EdocUR - U. Rosario
- Idioma:
- eng
- OAI Identifier:
- oai:repository.urosario.edu.co:10336/23667
- Acceso en línea:
- https://doi.org/10.1111/ced.12627
https://repository.urosario.edu.co/handle/10336/23667
- Palabra clave:
- Adult
Amplicon
Article
Autosomal recessive congenital ichthyosis
Case report
Exon skipping
Female
Gene
Gene mutation
Gene rearrangement
Genetic counseling
Genotype
Genotype phenotype correlation
Human
Ichthyosis
Intron
Intron retention
Phenotype
Physical examination
Priority journal
Single nucleotide polymorphism
Stop codon
Tgm1 gene
Congenital ichthyosiform erythroderma
Genetic predisposition
Genetics
Mutation
Recessive gene
Rna splicing
Protein glutamine gamma glutamyltransferase
Rna splicing
Transglutaminase 1
Adult
Female
Genetic predisposition to disease
Humans
Mutation
Rna splice sites
Transglutaminases
congenital
recessive
Genes
Ichthyosiform erythroderma
- Rights
- License
- Abierto (Texto Completo)