Clinical heterogeneity within xeroderma pigmentosum associated with mutations in the DNA repair and transcription gene ERCC3

Keyphrases

• DNA Repair 100%
• DNA Transcription 100%
• Xeroderma pigmentosum 100%
• Clinical Heterogeneity 100%
• ERCC3 100%
• Nucleotide Excision Repair 71%
• Failed Repair 42%
• DNA Repair Genes 28%
• Mutation Frequency 14%
• Clinical Features 14%
• Autosomal Recessive 14%
• T Cells 14%
• Missense mutation 14%
• Molecular Analysis 14%
• DNA Excision Repair 14%
• Cockayne Syndrome 14%
• Blood Samples 14%
• Drosophilidae 14%
• Single-base Substitution 14%
• In Vivo mutation 14%
• Late-onset 14%
• Single Patient 14%
• TFIIH 14%
• Complementation Group 14%
• Transcription Initiation 14%
• Human DNA 14%
• Skin Tumor 14%
• DNA Helicase 14%
• Transcription Factor Complex 14%
• Cutaneous Symptoms 14%
• Hprt 14%
• Cutaneous Tumors 14%
• Microneedle Injection 14%
• Neurological Impairment 14%
• DNA Repair-deficiency Disorders 14%
• Vital Process 14%

Biochemistry, Genetics and Molecular Biology

• Base Excision Repair 100%
• DNA Repair 100%
• DNA Transcription 100%
• Nucleotide Excision Repair 100%
• Xeroderma pigmentosum 100%
• Gene Transcription 100%
• Gene Repair 33%
• Transcription 33%
• Allele 16%
• T Cell 16%
• Mutation Rate 16%
• Autosomal Recessive Inheritance 16%
• Missense Mutation 16%
• Cockayne Syndrome 16%
• Helicase 16%
• Nucleic Acid Base Substitution 16%
• Transcription Factor IIH 16%
• Xerodermum Pigmentosum B 16%
• Cell Hybridization 16%
• Class II Gene 16%

Medicine and Dentistry

• Base Excision Repair 100%
• DNA Repair 100%
• DNA Transcription 100%
• Xeroderma pigmentosum 100%
• Gene Transcription 100%
• Gene Repair 33%
• Skin Tumor 33%
• Allele 16%
• Base 16%
• Clinical Feature 16%
• Autosomal Recessive Inheritance 16%
• T Lymphocyte 16%
• Cockayne Syndrome 16%
• Mutation Rate 16%
• Missense Mutation 16%
• Transcription Factor IIH 16%
• DNA Helicase 16%
• Hypoxanthine Phosphoribosyltransferase 16%
• Cell Hybridization 16%
• Disorders of DNA Synthesis and Repair 16%