RP2 and RPGR Mutations and Clinical Correlations in Patients with X-Linked Retinitis Pigmentosa

American Journal of Human Genetics

Volumn 73, Issue 5, 2003, Pages 1131-1146

  Sharon, Dror ^a,b   Sandberg, Michael A ^a   Rabe, Vivian W ^a   Stillberger, Melissa ^a   Dryja, Thaddeus P ^a   Berson, Eliot L ^a  

^a MASSACHUSETTS EYE AND EAR INFIRMARY   (United States)

^b HADASSAH HEBREW UNIVERSITY MEDICAL CENTER   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID;

AMINO ACID SEQUENCE; ANALYTIC METHOD; ARTICLE; CONTROLLED STUDY; CORRELATION ANALYSIS; DARK ADAPTATION; DISEASE SEVERITY; ELECTRORETINOGRAM; EXON; FRAMESHIFT MUTATION; GENE; GENE IDENTIFICATION; GENE MUTATION; GENE SEQUENCE; GENETIC SCREENING; HUMAN; MAJOR CLINICAL STUDY; MALE; MEASUREMENT; MUTATIONAL ANALYSIS; PATIENT; PRIORITY JOURNAL; REFRACTION ERROR; REGRESSION ANALYSIS; RETINA CONE; RETINA DEGENERATION; RETINA ROD; RETINITIS PIGMENTOSA; RP2 GENE; RPGR GENE; SEQUENCE ANALYSIS; VISUAL ACUITY; VISUAL FIELD; WILD TYPE; X CHROMOSOME ABERRATION;

STAPHYLOCOCCUS PHAGE 187;

EID: 0242522448     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/379379     Document Type: Article

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