SCOPUS 정보 검색 플랫폼

Biochemical and Biophysical Research Communications

Volumn 277, Issue 3, 2000, Pages 771-775

Mitochondrial DNA variations in patients with maternally inherited diabetes and deafness syndrome

(8) Perucca Lostanlen, D a Narbonne, H b Hernandez, J B a Staccini, P a Saunieres, A a Paquis Flucklinger, V a Vialettes, B b Desnuelle, C a

a CNRS (France)

b HÔPITAL SAINTE MARGUERITE (France)

Author keywords

Mitochondrial diabetes; Mitochondrial DNA; Point mutations

Indexed keywords

LEUCINE TRANSFER RNA; MITOCHONDRIAL DNA;

ADULT; AGED; ARTICLE; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; DIABETES MELLITUS; DNA DETERMINATION; EXTRACHROMOSOMAL INHERITANCE; GENE MUTATION; GENE SEQUENCE; GENETIC VARIABILITY; HEARING IMPAIRMENT; HUMAN; HUMAN TISSUE; MATERNALLY INHERITED DIABETES AND DEAFNESS; PRIORITY JOURNAL;

EID: 0034597744 PISSN: 0006291X EISSN: None Source Type: Journal
DOI: 10.1006/bbrc.2000.3751 Document Type: Article

Times cited : (24)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.