Survey of CAG/CTG repeats in human cDNAs representing new genes: Candidates for inherited neurological disorders

Human Molecular Genetics

Volumn 5, Issue 7, 1996, Pages 1001-1009

  Néri, Christian ^a   Albanèse, Véronique ^a   Lebre, Anne Sophie ^a   Holbert, Sébastien ^a   Saada, Claudine ^a   Bougueleret, Lydie ^a   Meier Ewert, Sebastian ^b   Le Gall, Isabelle ^a   Millasseau, Philippe ^a   Bui, Hung ^a   Giudicelli, Catherine ^a   Massart, Catherine ^a   Guillou, Sophie ^a   Gervy, Patricia ^a   Poullier, Eric ^a   Rigault, Philippe ^a   Weissenbach, Jean ^c   Lennon, Greg ^d   Chumakov, Ilya ^a   Dausset, Jean ^a   Lehrach, Hans ^b   Cohen, Daniel ^a   Cann, Howard M ^a   more..

^a FONDATION JEAN DAUSSET CEPH   (France)

^b MAX PLANCK INSTITUTE FOR MOLECULAR GENETICS   (Germany)

^c GÉNÉTHON   (France)

^d LAWRENCE LIVERMORE NATIONAL LABORATORY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; REPETITIVE DNA;

ANIMAL CELL; ARTICLE; CHROMOSOME 12Q; CHROMOSOME 13Q; CHROMOSOME 19Q; CHROMOSOME 1Q; CHROMOSOME 3P; CHROMOSOME 4Q; CODON; DEGENERATIVE DISEASE; GENETIC POLYMORPHISM; HETEROZYGOTE; HUMAN; HUMAN CELL; NEUROLOGIC DISEASE; NEUROMUSCULAR DISEASE; NEUROPSYCHIATRY; NONHUMAN; PRIORITY JOURNAL; YEAST ARTIFICIAL CHROMOSOME;

BRAIN; BRAIN CHEMISTRY; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN; CLONING, MOLECULAR; DNA, COMPLEMENTARY; GENE EXPRESSION; GENE LIBRARY; GENES; HUMANS; INFANT, NEWBORN; MOLECULAR SEQUENCE DATA; NERVOUS SYSTEM DISEASES; POLYMORPHISM, GENETIC; SEQUENCE ANALYSIS, DNA; TRINUCLEOTIDE REPEATS;

EID: 8944262197     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/5.7.1001     Document Type: Article

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