SCOPUS 정보 검색 플랫폼

Volumn 69, Issue 1, 2001, Pages 228-234

A common ancestral origin of the frequent and widespread 2299delG USH2A mutation

(9) Dreyer, Bo a Tranebjærg, Lisbeth a Brox, Vigdis a Rosenberg, Thomas b Möller, Claes c Beneyto, Magdalena d Weston, Michael D e Kimberling, William J e Nilssen, Øivind a

a UNIVERSITY HOSPITAL OF NORTH NORWAY (Norway)

b JOHN F KENNEDY INSTITUTE (Denmark)

c SAHLGRENSKA UNIVERSITY HOSPITAL (Sweden)

d HOSPITAL UNIVERSITARIO LA FE (Spain)

e Boystown National Research Hospital (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; DISEASE ASSOCIATION; DISEASE SEVERITY; EUROPE; GENE MUTATION; GENETIC MARKER; GENOTYPE; GEOGRAPHY; HAPLOTYPE; HEARING LOSS; HUMAN; MAJOR CLINICAL STUDY; MIGRATION; NORTH AMERICA; POLYMERASE CHAIN REACTION; PREVALENCE; PRIORITY JOURNAL; RETINITIS PIGMENTOSA; SINGLE NUCLEOTIDE POLYMORPHISM; USHER SYNDROME; VISUAL IMPAIRMENT;

EID: 0034973570 PISSN: 00029297 EISSN: None Source Type: Journal
DOI: 10.1086/321269 Document Type: Article

Times cited : (69)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.