Clinical features of X linked juvenile retinoschisis in Chinese families associated with novel mutations in the RS1 gene

Molecular Vision

Volumn 13, Issue , 2007, Pages 804-812

  Li, Xiaoxin ^a   Ma, Xiang ^a   Tao, Yong ^a  

^a PEKING UNIVERSITY PEOPLE S HOSPITAL   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; ASPARTIC ACID; CYSTEINE; CYTOSINE; GLUTAMINE; GLYCINE; GUANINE; HISTIDINE; MUTANT PROTEIN; PROLINE; RETINOSCHISIN; RS1 PROTEIN; SERINE; THYMINE; TRYPTOPHAN; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; ARTICLE; CHILD; CHINESE; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; DISEASE SEVERITY; EARLY DIAGNOSIS; EXON; EYE EXAMINATION; FAMILY; FEMALE; FRAMESHIFT MUTATION; GENE AMPLIFICATION; GENETIC COUNSELING; GENETIC POLYMORPHISM; GENOTYPE PHENOTYPE CORRELATION; HETEROZYGOSITY; HUMAN; MALE; MISSENSE MUTATION; MUTATIONAL ANALYSIS; PEDIGREE ANALYSIS; PHENOTYPIC VARIATION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROGNOSIS; RETINA FOVEA; RETINOSCHISIS; SEQUENCE ANALYSIS; TREATMENT PLANNING; X CHROMOSOME LINKED DISORDER;

ADOLESCENT; ADULT; AGED; ASIAN CONTINENTAL ANCESTRY GROUP; BASE SEQUENCE; CHILD; CHINA; DNA MUTATIONAL ANALYSIS; EXONS; EYE PROTEINS; FEMALE; FUNDUS OCULI; HUMANS; MALE; MIDDLE AGED; MOLECULAR SEQUENCE DATA; MUTATION; PEDIGREE; REFRACTIVE ERRORS; RETINOSCHISIS;

EID: 34250173847     PISSN: None     EISSN: 10900535     Source Type: Journal    
DOI: None     Document Type: Article

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