Genetic etiology study of the non-syndromic deafness in Chinese Hans by targeted next-generation sequencing

Orphanet Journal of Rare Diseases

Volumn 8, Issue 1, 2013, Pages

  Yang, Tao ^a,b   Wei, Xiaoming ^c   Chai, Yongchuan ^a,b   Li, Lei ^a,b   Wu, Hao ^a,b  

^a SHANGHAI JIAO TONG UNIVERSITY   (China)

^b SHANGHAI JIAO TONG UNIVERSITY SCHOOL OF MEDICINE   (China)

^c BGI SHENZHEN   (China)

Author keywords

Deafness; Genetic etiology; Non syndromic; Targeted next generation sequencing

Indexed keywords

CONNEXIN 26; PENDRIN;

ADOLESCENT; ADULT; ALLELE; ARTICLE; CHILD; CHINESE; EXON; FEMALE; GENE MUTATION; GENE SEQUENCE; GENE TARGETING; GENETIC SCREENING; GENETIC VARIABILITY; HEARING IMPAIRMENT; HUMAN; INFANT; MAJOR CLINICAL STUDY; MALE; NEWBORN; PRESCHOOL CHILD; SCHOOL CHILD;

ADOLESCENT; ALLELES; ASIAN CONTINENTAL ANCESTRY GROUP; CHILD; CONNEXINS; DEAFNESS; FEMALE; GENETIC LINKAGE; HEARING LOSS, SENSORINEURAL; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; MALE; MUTATION; PEDIGREE;

EID: 84878895417     PISSN: None     EISSN: 17501172     Source Type: Journal    
DOI: 10.1186/1750-1172-8-85     Document Type: Article

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