A Novel EYA1 Mutation Causing Alternative RNA Splicing in a Chinese Family With Branchio-Oto Syndrome: Implications for Molecular Diagnosis and Clinical Application

논문상세정보
' A Novel EYA1 Mutation Causing Alternative RNA Splicing in a Chinese Family With Branchio-Oto Syndrome: Implications for Molecular Diagnosis and Clinical Application' 의 주제별 논문영향력
논문영향력 선정 방법
논문영향력 요약
주제
  • Alternative Splicing
  • Correction of Hearing Impairment
  • EYA1
  • Hearing Loss
동일주제 총논문수 논문피인용 총횟수 주제별 논문영향력의 평균
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