Mutations of 60 known causative genes in 157 families with retinitis pigmentosa based on exome sequencing.

Human genetics

Volumn 133, Issue 10, 2014, Pages 1255-1271

  Xu, Yan ^a   Guan, Liping ^b   Shen, Tao ^b   Zhang, Jianguo ^b   Xiao, Xueshan ^b   Jiang, Hui ^b   Li, Shiqiang ^b   Yang, Jianhua ^b   Jia, Xiaoyun ^b   Yin, Y ^b   Guo, Xiangming ^b   Wang, Jun ^b   Zhang, Qingjiong ^b  

^a SUN YAT SEN UNIVERSITY   (China)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AGED; ARTICLE; ASIAN; CASE CONTROL STUDY; CHILD; EXOME; FAMILY; FEMALE; GENE FREQUENCY; GENETIC PREDISPOSITION; GENETICS; HUMAN; MALE; METHODOLOGY; MIDDLE AGED; MUTATION; NUCLEOTIDE SEQUENCE; PEDIGREE; PRESCHOOL CHILD; RETINITIS PIGMENTOSA; YOUNG ADULT;

ADOLESCENT; ADULT; AGED; ASIAN CONTINENTAL ANCESTRY GROUP; CASE-CONTROL STUDIES; CHILD; CHILD, PRESCHOOL; DNA MUTATIONAL ANALYSIS; EXOME; FAMILY; FEMALE; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; MIDDLE AGED; MUTATION; PEDIGREE; RETINITIS PIGMENTOSA; YOUNG ADULT;

EID: 84910111705     PISSN: None     EISSN: 14321203     Source Type: Journal    
DOI: 10.1007/s00439-014-1460-2     Document Type: Article

References (0)