Novel recessive mutations of COL6A1 identified in the early severe phenotype of ullrich congenital muscular dystrophy

논문상세정보
' Novel recessive mutations of COL6A1 identified in the early severe phenotype of ullrich congenital muscular dystrophy' 의 주제별 논문영향력
논문영향력 선정 방법
논문영향력 요약
주제
  • 질병
  • Collagen type VI
  • muscular dystrophy
  • phenotype
동일주제 총논문수 논문피인용 총횟수 주제별 논문영향력의 평균
861 0

0.0%