A review of the molecular genetics of congenital idiopathic nystagmus (CIN)

Ophthalmic Genetics

Volumn 28, Issue 4, 2007, Pages 187-191

  Self, James ^a   Lotery, Andrew ^b  

^a SOUTHAMPTON GENERAL HOSPITAL   (United Kingdom)

^b NONE

Author keywords

FRMD7; Genetics; Nystagmus

Indexed keywords

AUTOSOMAL DOMINANT INHERITANCE; CELL SELECTION; CONGENITAL NYSTAGMUS; GENE IDENTIFICATION; GENE LOCUS; GENE MUTATION; GENETIC LINKAGE; HUMAN; MOLECULAR GENETICS; PEDIGREE ANALYSIS; PRIORITY JOURNAL; REVIEW;

FEMALE; GENES, DOMINANT; GENES, RECESSIVE; GENETIC DISEASES, X-LINKED; GENETIC PREDISPOSITION TO DISEASE; HAPLOTYPES; HUMANS; MALE; NYSTAGMUS, CONGENITAL; PEDIGREE;

EID: 37649004248     PISSN: 13816810     EISSN: 17445094     Source Type: Journal    
DOI: 10.1080/13816810701651233     Document Type: Review

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