Complexity of phenotype-genotype correlations in Spanish patients with RDH12 mutations

Investigative Ophthalmology and Visual Science

Volumn 50, Issue 3, 2009, Pages 1065-1068

  Valverde, Diana ^a   Pereiro, Ines ^a   Vallespín, Elena ^b   Ayuso, Carmen ^b   Borrego, Salud ^c   Baiget, Montserrat ^d  

^a UNIVERSITY OF VIGO   (Spain)

^b Hospital UniversitarioFundación Jiménez Díaz   (Spain)

^c HOSPITAL UNIVERSITARIO VIRGEN DEL ROCÍO   (Spain)

^d HOSPITAL DE LA SANTA CREU I SANT PAU   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

11 CIS RETINAL; DNA FRAGMENT; OXIDOREDUCTASE; RETINOL DEHYDROGENASE 12; UNCLASSIFIED DRUG; ALCOHOL DEHYDROGENASE; RDH12 PROTEIN, HUMAN;

ARTICLE; CHILD; CHROMATOPHORE; CLINICAL ARTICLE; CONTROLLED STUDY; GENE MUTATION; GENOTYPE; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; LEBER CONGENITAL AMAUROSIS; PHENOTYPE; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; SPAIN; VISUAL ACUITY; ADULT; BLINDNESS; GENETICS; MIDDLE AGED; MUTATION; RETINA DEGENERATION; VISUAL FIELD;

ADULT; ALCOHOL OXIDOREDUCTASES; BLINDNESS; CHILD; CHILD, PRESCHOOL; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; GENOTYPE; HUMANS; MIDDLE AGED; MUTATION; PHENOTYPE; RETINAL DEGENERATION; SPAIN; VISUAL ACUITY; VISUAL FIELDS;

EID: 62649164796     PISSN: 01460404     EISSN: 15525783     Source Type: Journal    
DOI: 10.1167/iovs.08-2083     Document Type: Article

References (10)

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