Investigation of the gene mutations in two Chinese families with X-linked infantile nystagmus

Molecular Vision

Volumn 17, Issue , 2011, Pages 461-468

  Li, Ningdong ^a,b   Wang, Xiaojuan ^a,c   Wang, Yuchuan ^b   Wang, Liming ^b   Ying, Ming ^b   Han, Ruifang ^a   Liu, Yuyan ^a   Zhao, Kanxing ^a,b  

^a TIANJIN MEDICAL UNIVERSITY   (China)

^b TIANJIN EYE HOSPITAL   (China)

^c Xuzhou Eye Institute   (China)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID SEQUENCE; ARTICLE; CHINESE; CLINICAL ARTICLE; CONGENITAL NYSTAGMUS; CONTROLLED STUDY; EXON; FEMALE; FERM DOMAIN CONTAINING 7 GENE; GENE; GENE AMPLIFICATION; GENE MUTATION; GENE SEQUENCE; GENETIC LINKAGE; HUMAN; MALE; MULTIPLEX LIGATION DEPENDENT PROBE AMPLIFICATION; MUTATIONAL ANALYSIS; NUCLEOTIDE SEQUENCE; PATHOGENESIS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RANDOM AMPLIFIED MICROSATELLITE; X CHROMOSOME LINKED DISORDER;

ADULT; AMINO ACID SEQUENCE; ASIAN CONTINENTAL ANCESTRY GROUP; BASE SEQUENCE; CYTOSKELETAL PROTEINS; DNA MUTATIONAL ANALYSIS; EYE MOVEMENTS; FAMILY; FEMALE; GENE DOSAGE; GENETIC DISEASES, X-LINKED; HUMANS; INFANT; MALE; MEMBRANE PROTEINS; MODELS, MOLECULAR; MOLECULAR SEQUENCE DATA; MUTATION; NYSTAGMUS, CONGENITAL; PEDIGREE; PROTEIN STRUCTURE, TERTIARY; SEQUENCE ALIGNMENT;

EID: 79952172309     PISSN: None     EISSN: 10900535     Source Type: Journal    
DOI: None     Document Type: Article

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