Deleterious mutations in the Zinc-Finger 469 gene cause brittle cornea syndrome

Keyphrases

• Deleterious mutations 100%
• Zinc Finger 100%
• Brittle Cornea Syndrome 100%
• Blindness 25%
• Jewish Population 25%
• Transcription Factor 25%
• Collagen 25%
• Systemic Symptoms 25%
• Autosomal Recessive 25%
• Disease Genes 25%
• Connective Tissue 25%
• Connective Tissue Disease 25%
• Single nucleotide Deletion 25%
• Hyperlaxity 25%
• Kyphoscoliosis 25%
• Hypermobility 25%
• Thin Cornea 25%
• Frameshift mutation 25%
• Progressive Visual Loss 25%
• Palestinian Family 25%
• Collagen Fibers 25%

Medicine and Dentistry

• Zinc Finger Protein 100%
• Disease 66%
• Amaurosis 33%
• Symptom 33%
• Connective Tissue 33%
• Visual Impairment 33%
• Connective Tissue Disease 33%
• Collagen Fiber 33%
• Kyphoscoliosis 33%
• Transcription Factors 33%
• Autosomal Recessive Disorder 33%
• Frameshift Mutation 33%

Immunology and Microbiology

• Connective Tissue 100%
• Autosomal Recessive Inheritance 50%
• Collagen Fiber 50%
• Transcription Factors 50%
• Frameshift Mutation 50%