The mitochondrial ND1 T3308C mutation in a Chinese family with the secondary hypertension

Biochemical and Biophysical Research Communications

Volumn 368, Issue 1, 2008, Pages 18-22

  Liu, Yuqi ^a   Li, Zongbin ^a   Yang, Li ^b   Wang, Shiwen ^a   Guan, Min Xin ^b,c  

^a CHINESE PLA GENERAL HOSPITAL   (China)

^b CINCINNATI CHILDREN'S HOSPITAL MEDICAL CENTER   (United States)

^c UNIVERSITY OF CINCINNATI COLLEGE OF MEDICINE   (United States)

Author keywords

Chinese; Hypertension; Mitochondrial DNA; Modifiers; Mutation; Processing; Renal; tRNA

Indexed keywords

AMINO ACID; METHIONINE; MITOCHONDRIAL DNA; RNA PRECURSOR; THREONINE; TRANSFER RNA;

ARTICLE; ASIAN; CHINESE; CLINICAL ASSESSMENT; CONTROLLED STUDY; DISEASE ASSOCIATION; DISORDERS OF MITOCHONDRIAL FUNCTIONS; FAMILY STUDY; GENE MUTATION; GENETIC ANALYSIS; HAPLOTYPE; HUMAN; HYPERTENSION; MITOCHONDRION; MOLECULAR GENETICS; NUCLEOTIDE SEQUENCE; PATHOGENESIS; PEDIGREE; PRIORITY JOURNAL; RENOVASCULAR HYPERTENSION; RNA TRANSLATION; SEQUENCE ANALYSIS;

ADULT; ASIAN CONTINENTAL ANCESTRY GROUP; BASE SEQUENCE; CYSTEINE; DNA, MITOCHONDRIAL; FEMALE; HUMANS; HYPERTENSION; MALE; MITOCHONDRIA; MOLECULAR SEQUENCE DATA; MUTATION; NADH DEHYDROGENASE; PEDIGREE; THREONINE;

EID: 39149139990     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2007.12.193     Document Type: Article

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