Fragile X syndrome and connective tissue dysregulation

Fragile X syndrome (FXS) is the most common cause of inherited intellectual disabilities and autism spectrum disorders, and it is an X-linked disorder in which there is a deficiency of the fragile X mental retardation 1 protein. This protein is crucial in regulating translation of mRNAs related to d...

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Autores:

Tipo de recurso:

Fecha de publicación:

2019

Institución:

Universidad del Rosario

Repositorio:

Repositorio EdocUR - U. Rosario

Idioma:

eng

OAI Identifier:

oai:repository.urosario.edu.co:10336/23681

Acceso en línea:

https://doi.org/10.1111/cge.13469
https://repository.urosario.edu.co/handle/10336/23681

Palabra clave:

Actin
Elastin
Gelatinase b
Minocycline
Fmr1 protein, human
Fragile x mental retardation protein
Scleroprotein
Cardiovascular system
Connective tissue disease
Fragile x syndrome
Human
Musculoskeletal system
Nonhuman
Priority journal
Review
Urogenital system
Animal
Antibody specificity
Connective tissue
Fragile x syndrome
Genetic association study
Genetic predisposition
Genetics
Metabolism
Organogenesis
Pathophysiology
Phenotype
Animals
Connective tissue
Extracellular matrix proteins
Fragile x mental retardation protein
Fragile x syndrome
Genetic association studies
Genetic predisposition to disease
Humans
Organ specificity
Organogenesis
Phenotype
Connective tissue
Extracellular matrix
Extracellular matrix proteins
Fragile x syndrome

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