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Cockayne syndrome: Clinical features, model systems and pathways
Ajoy C Karikkineth,
Morten Scheibye-Knudsen
, Elayne Fivenson, Deborah L Croteau,
Vilhelm A Bohr
Molecular Aging Program
Damage and Repair
Individualized Health
97
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Keyphrases
Feature Model
100%
Cockayne Syndrome
100%
Clinical Features
100%
Microcephaly
16%
Neurological Manifestations
16%
Progeria
16%
Accelerated Aging
16%
Nucleotide Excision Repair
16%
Dwarfism
16%
Autosomal Recessive
16%
Aging
16%
DNA Mitochondrial
16%
Complementation Group
16%
Molecular Intervention
16%
Aging Mechanism
16%
Cataract
16%
Feeding Difficulties
16%
Sensorineural Deafness
16%
DNA Repair Capacity
16%
Cognitive Deficits
16%
Xeroderma pigmentosum
16%
Mitochondrial Function
16%
Medicine and Dentistry
Cockayne Syndrome
100%
Clinical Feature
100%
Autosomal Recessive Disorder
16%
Sensorineural Hearing Loss
16%
DNA Repair
16%
Neurologic Finding
16%
Cataract
16%
Microcephaly
16%
Progeria
16%
Base
16%
Diseases
16%
Mitochondrial DNA
16%
Xeroderma pigmentosum
16%
Prevalence
16%
Retinopathy
16%
Base Excision Repair
16%
Accelerated Aging
16%
Cognitive Defect
16%
Biochemistry, Genetics and Molecular Biology
Cockayne Syndrome
100%
Transcription
33%
Mitochondrial DNA
16%
Base Excision Repair
16%
Molecular Intervention
16%
Nucleotide Excision Repair
16%
DNA Repair
16%
Autosomal Recessive Disorder
16%
Prevalence
16%
Xeroderma pigmentosum
16%
Progeria
16%
Neuroscience
Cockayne Syndrome
100%
Cognitive Disorder
16%
Nucleotide Excision Repair
16%
Mitochondrial Function
16%
Mitochondrial DNA
16%
Retinal Disease
16%
Autosomal Recessive Disorder
16%
Cataract
16%
Base Excision Repair
16%
Microcephaly
16%