Analysis of the CHN1 gene in patients with various types of congenital ocular motility disorders

Graefe's Archive for Clinical and Experimental Ophthalmology

Volumn 248, Issue 9, 2010, Pages 1351-1357

  Volk, Alexander E ^a,b   Fricke, Julia ^a   Strobl, Judith ^a   Kolling, Gerold ^c   Kubisch, Christian ^a,b   Neugebauer, Antje ^a  

^a UNIVERSITY HOSPITAL OF COLOGNE   (Germany)

^b UNIVERSITY OF COLOGNE   (Germany)

^c UNIVERSITY HOSPITAL HEIDELBERG   (Germany)

Author keywords

CCDD; CHN1; Congenital ocular motility disorders; Duane's retraction syndrome

Indexed keywords

CHIMERIN;

5' UNTRANSLATED REGION; ADOLESCENT; AMINO ACID SUBSTITUTION; ARTICLE; BROWN SYNDROME; CHILD; CLINICAL ARTICLE; CONVERGENT STRABISMUS; DNA DETERMINATION; DNA POLYMORPHISM; DUANE RETRACTION SYNDROME; EXON; EYE MOVEMENT DISORDER; FAMILY HISTORY; FEMALE; GENE MUTATION; GENETIC HETEROGENEITY; HETEROZYGOSITY; HUMAN; INTRON; MALE; MUTATIONAL ANALYSIS; NYSTAGMUS; PRIORITY JOURNAL; SCHOOL CHILD;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; CHIMERIN 1; DNA MUTATIONAL ANALYSIS; DUANE RETRACTION SYNDROME; FEMALE; GENETIC HETEROGENEITY; HUMANS; MALE; MIDDLE AGED; MUTATION; OCULAR MOTILITY DISORDERS; POLYMERASE CHAIN REACTION; TRANSCRIPTION FACTORS;

EID: 77955552850     PISSN: 0721832X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00417-010-1417-7     Document Type: Article

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