메뉴 건너뛰기




Volumn 47, Issue 3, 2001, Pages 491-497

Double-gradient denaturing gradient gel electrophoresis assay for identification of L-ferritin iron-responsive element mutations responsible for hereditary hyperferritinemia-cataract syndrome: Identification of the new mutation Cl4G

Author keywords

[No Author keywords available]

Indexed keywords

DNA; FERRITIN; MESSENGER RNA;

EID: 0035103330     PISSN: 00099147     EISSN: None     Source Type: Journal    
DOI: 10.1093/clinchem/47.3.491     Document Type: Article
Times cited : (35)

References (33)
  • 25
  • 26
    • 0034210637 scopus 로고    scopus 로고
    • Translational pathophysiology: A novel molecular mechanism of human disease
    • (2000) Blood , vol.95 , pp. 3280-3288
    • Cazzola, M.1    Skoda, R.C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.