Crumbs homolog 1 (CRB1) mutations result in a thick human retina with abnormal lamination

Human Molecular Genetics

Volumn 12, Issue 9, 2003, Pages 1073-1078

  Jacobson, Samuel G ^a   Cideciyan, Artur V ^a   Aleman, Tomas S ^a   Pianta, Michael J ^a   Sumaroka, Alexander ^a   Schwartz, Sharon B ^a   Smilko, Elaine E ^a   Milam, Ann H ^a   Sheffield, Val C ^b   Stone, Edwin M ^b  

^a UNIVERSITY OF PENNSYLVANIA   (United States)

^b UNIVERSITY OF IOWA HOSPITALS AND CLINICS   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MEMBRANE PROTEIN;

ADOLESCENT; ADULT; APOPTOSIS; AUTOSOMAL RECESSIVE DISORDER; BLINDNESS; CELL POLARITY; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; DROSOPHILA; EPITHELIUM CELL; FEMALE; GENE MUTATION; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; IN VIVO STUDY; MALE; MORPHOGENESIS; OPTIC NERVE; PHOTORECEPTOR; PRIORITY JOURNAL; RETINA DEVELOPMENT; RETINA DISEASE; REVIEW;

EYE PROTEINS; HUMANS; MALE; MEMBRANE PROTEINS; MIDDLE AGED; NERVE TISSUE PROTEINS; OPTIC NERVE; RETINA;

EID: 0038364012     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/ddg117     Document Type: Review

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