지원사업
학술연구/단체지원/교육 등 연구자 활동을 지속하도록 DBpia가 지원하고 있어요.
커뮤니티
연구자들이 자신의 연구와 전문성을 널리 알리고, 새로운 협력의 기회를 만들 수 있는 네트워킹 공간이에요.
논문 기본 정보
- 자료유형
- 학술저널
- 저자정보
- 저널정보
- 대한이비인후과학회 Clinical and Experimental Otorhinolaryngology Clinical and Experimental Otorhinolaryngology 제13권 제2호
- 발행연도
- 2020.1
- 수록면
- 87 - 88 (2page)
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참고문헌 (9)
참고문헌 신청
Bonnet C / 2012 / Usher syndrome(sensorineural deafness and retinitis pigmentosa) : pathogenesis, molecular diagnosis and therapeutic approaches / Curr Opin Neurol 25(1):42~49
Boughman JA / 1983 / Usher syndrome : definition and estimate of prevalence from two high-risk populations / J Chronic Dis 36(8):595~603
Kimberling WJ / 2010 / Frequency of Usher syndrome in two pediatric populations : implications for genetic screening of deaf and hard of hearing children / Genet Med 12(8):512~516
이상연 / 2020 / Severe or Profound Sensorineural Hearing Loss Caused by Novel USH2A Variants in Korea: Potential Genotype-Phenotype Correlation / Clinical and Experimental Otorhinolaryngology 13(2):113~122
Eandi CM / 2017 / Targeted next generation sequencing in Italian patients with Usher syndrome : phenotype-genotype correlations / Sci Rep 7(1):15681
Boughman JA / 1983 / Usher syndrome : definition and estimate of prevalence from two high-risk populations / J Chronic Dis 36(8):595~603
Kimberling WJ / 2010 / Frequency of Usher syndrome in two pediatric populations : implications for genetic screening of deaf and hard of hearing children / Genet Med 12(8):512~516
이상연 / 2020 / Severe or Profound Sensorineural Hearing Loss Caused by Novel USH2A Variants in Korea: Potential Genotype-Phenotype Correlation / Clinical and Experimental Otorhinolaryngology 13(2):113~122
Eandi CM / 2017 / Targeted next generation sequencing in Italian patients with Usher syndrome : phenotype-genotype correlations / Sci Rep 7(1):15681
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