Familial discordance in stargardt disease

Molecular Vision

Volumn 18, Issue , 2012, Pages 227-233

  Burke, Tomas R ^a,c   Tsang, Stephen H ^a   Zernant, Jana ^a   Smith, R Theodore ^a,b   Allikmets, Rando ^a  

^a New York Presbyterian Hospital   (United States)

^b King Edward VII Hospital ^*  (United States)

^c KING EDWARD VII HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ALLELE; ARTICLE; ATP BINDING CASSETTE TRANSPORTER SUBFAMILY A MEMBER 4 GENE; AUTOFLUORESCENCE; CLINICAL ARTICLE; CLINICAL ASSESSMENT; CONTROLLED STUDY; DISEASE SEVERITY; ELECTRORETINOGRAPHY; FEMALE; GENE; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; HETEROZYGOSITY; HUMAN; MALE; MICROARRAY ANALYSIS; MUTATIONAL ANALYSIS; ONSET AGE; PATHOGENICITY; PHENOTYPIC VARIATION; PLEIOTROPY; PRIORITY JOURNAL; SPECTRAL DOMAIN OPTICAL COHERENCE TOMOGRAPHY; STARGARDT DISEASE; VISUAL ACUITY;

ADULT; ALLELES; ATP-BINDING CASSETTE TRANSPORTERS; CORNEAL DYSTROPHIES, HEREDITARY; DNA MUTATIONAL ANALYSIS; ELECTRORETINOGRAPHY; FEMALE; GENES, RECESSIVE; GENOTYPE; HETEROZYGOTE; HUMANS; MALE; MIDDLE AGED; MUTATION; PEDIGREE; PHENOTYPE; PROTEIN STRUCTURE, TERTIARY; SEVERITY OF ILLNESS INDEX; TOMOGRAPHY, OPTICAL COHERENCE;

EID: 84863073389     PISSN: None     EISSN: 10900535     Source Type: Journal    
DOI: None     Document Type: Article

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