Novel frameshift mutations in CRX associated with Leber congenital amaurosis

Human mutation

Volumn 18, Issue 6, 2001, Pages 550-551

  Rivolta, Carlo ^a   Peck, Naomi E ^a   Fulton, Anne B ^b   Fishman, Gerald A ^c   Berson, Eliot L ^a   Dryja, Thaddeus P ^a  

^a MASSACHUSETTS EYE AND EAR INFIRMARY   (United States)

^b BOSTON CHILDREN S HOSPITAL   (United States)

^c UNIVERSITY OF ILLINOIS AT CHICAGO   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CONE ROD HOMEOBOX PROTEIN; DNA; HOMEODOMAIN PROTEIN; TRANSACTIVATOR PROTEIN;

ARTICLE; CHEMISTRY; FEMALE; FRAMESHIFT MUTATION; GENETICS; GENOTYPE; HUMAN; LEBER HEREDITARY OPTIC NEUROPATHY; MALE; NUCLEOTIDE SEQUENCE;

DNA; DNA MUTATIONAL ANALYSIS; FEMALE; FRAMESHIFT MUTATION; GENOTYPE; HOMEODOMAIN PROTEINS; HUMANS; MALE; OPTIC ATROPHY, HEREDITARY, LEBER; TRANS-ACTIVATORS;

EID: 0035651286     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.1243     Document Type: Article

References (0)