Maternally inherited hearing loss is associated with the novel mitochondrial tRNASer(UCN) 7505T>C mutation in a Han Chinese family

Molecular Genetics and Metabolism

Volumn 100, Issue 1, 2010, Pages 57-64

  Tang, Xiaowen ^a   Li, Ronghua ^b   Zheng, Jing ^a   Cai, Qin ^a   Zhang, Ting ^a   Gong, Shasha ^a   Zheng, Wuwei ^a   He, Xiumei ^a   Zhu, Yi ^a,c   Xue, Ling ^a   Yang, Aifen ^a   Yang, Li ^b   Lu, Jianxin ^a   Guan, Min Xin ^a,b,d  

^a ZHEJIANG UNIVERSITY SCHOOL OF MEDICINE   (China)

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

^c WENZHOU MEDICAL UNIVERSITY   (China)

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

Author keywords

Chinese; Hearing loss; Maternally inherited; Metabolism; Mitochondrial; Mutation; tRNA

Indexed keywords

MITOCHONDRIAL DNA; TRANSFER RNA;

ADOLESCENT; ADULT; ARTICLE; CHILD; CHINESE; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE SEVERITY; EXTRACHROMOSOMAL INHERITANCE; FEMALE; GENE MUTATION; GENOTYPE; HEARING LOSS; HUMAN; MALE; NUCLEOTIDE SEQUENCE; ONSET AGE; PEDIGREE; PRIORITY JOURNAL; WILD TYPE;

ADOLESCENT; AGE OF ONSET; ASIAN CONTINENTAL ANCESTRY GROUP; CONNEXINS; DNA, MITOCHONDRIAL; FEMALE; HEARING LOSS, SENSORINEURAL; HUMANS; MALE; MITOCHONDRIAL PROTEINS; MUTATION; PEDIGREE; RNA, TRANSFER, AMINO ACYL; TRNA METHYLTRANSFERASES;

EID: 77950520149     PISSN: 10967192     EISSN: 10967206     Source Type: Journal    
DOI: 10.1016/j.ymgme.2010.01.008     Document Type: Article

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