A novel locus (CORD12) for autosomal dominant cone-rod dystrophy on chromosome 2q24.2-2q33.1

BMC Medical Genetics

Volumn 12, Issue , 2011, Pages

  Manes, Gaël ^a,b   Hebrard, Maxime ^a,b   Bocquet, Béatrice ^a,b   Meunier, Isabelle ^c   Coustes Chazalette, Delphine ^c   Sénéchal, Audrey ^a,b   Bolland Augé, Anne ^d   Zelenika, Diana ^d   Hamel, Christian P ^a,b,c  

^a Montpellier University Medical Center   (France)

^b UNIV MONTPELLIER   (France)

^c MONTPELLIER UNIVERSITY HOSPITAL   (France)

^d CENTRE NATIONAL DE GÉNOTYPAGE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHILD; CHROMOSOME 2Q; CLINICAL ARTICLE; FEMALE; FRANCE; GENE IDENTIFICATION; GENE LOCUS; GENE MAPPING; GENOME ANALYSIS; GENOTYPE; HUMAN; LINKAGE ANALYSIS; MALE; MICROSATELLITE MARKER; MUTATIONAL ANALYSIS; OPHTHALMOSCOPY; PEDIGREE; RETINA CONE ROD DYSTROPHY; RETINA DYSTROPHY; RETINITIS PIGMENTOSA; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM; CHROMOSOME 2; CHROMOSOME MAP; DOMINANT GENE; GENETIC LINKAGE; GENETICS; MIDDLE AGED;

MICROSATELLITE DNA;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 2; FEMALE; GENES, DOMINANT; GENETIC LINKAGE; HUMANS; MALE; MICROSATELLITE REPEATS; MIDDLE AGED; PEDIGREE; POLYMORPHISM, SINGLE NUCLEOTIDE; RETINITIS PIGMENTOSA;

EID: 79955090749     PISSN: None     EISSN: 14712350     Source Type: Journal    
DOI: 10.1186/1471-2350-12-54     Document Type: Article

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