关键词: COL11A1 COL2A1 Stickler syndrome de novo mutations high myopia retinal detachment
Mesh : Adult Arthritis / genetics pathology Child Collagen Type II / genetics Collagen Type XI / genetics Connective Tissue Diseases / genetics pathology Female Hearing Loss, Sensorineural / genetics pathology Humans Male Mutation Myopia / genetics pathology Pedigree Retinal Detachment / genetics pathology
来 源:
DOI:10.3390/genes11080882
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