The 1.4-Mb CMT1A duplication/HNPP deletion genomic region reveals unique genome architectural features and provides insights into the recent evolution of new genes

Genome Research

Volumn 11, Issue 6, 2001, Pages 1018-1033

  Inoue, Ken ^a   Dewar, Ken ^b   Katsanis, Nicholas ^a   Reiter, Lawrence T ^a,c   Lander, Eric S ^b   Devon, Keri L ^b   Wyman, Dudley W ^b   Lupski, James R ^a   Birren, Bruce ^b  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

^b WHITEHEAD INSTITUTE FOR BIOMEDICAL RESEARCH   (United States)

^c UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CGI 148 PROTEIN; CMT1A DUPLICATED REGION TRANSCRIPT 1; CMT1A DUPLICATED REGION TRANSCRIPT 15; CONTIG; CYCLOPHILIN A; DNA; HEPARAN SULFATE DEXTRO GLUCOSAMINYL 3 O SULFOTRANSFERASE 3B1; MEMBRANE PROTEIN; MYELIN PROTEIN; NPD008 PROTEIN; NUCLEOTIDE; PERIPHERAL MYELIN PROTEIN 22; POLYMER; SULFOTRANSFERASE; TEKTIN 3; TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG;

ARTICLE; BACTERIAL ARTIFICIAL CHROMOSOME; CHROMOSOME 17P; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CHROMOSOME MAP; CHROMOSOME STRUCTURE; CONTROLLED STUDY; EMBRYO DEVELOPMENT; EVOLUTION; FEMALE; GENDER; GENE REARRANGEMENT; GENETIC DISORDER; GENETIC RECOMBINATION; GENETIC SUSCEPTIBILITY; HEREDITARY MOTOR SENSORY NEUROPATHY; HETEROZYGOSITY; HYPOTHESIS; MALE; MEIOSIS; NONHUMAN; NUCLEOTIDE SEQUENCE; PARASITE; PERIPHERAL NEUROPATHY; PREDICTION; PRIMATE; PRIORITY JOURNAL; SPECIES DIFFERENTIATION;

ANIMALS; CHARCOT-MARIE-TOOTH DISEASE; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 17; EVOLUTION, MOLECULAR; FEMALE; GENE DOSAGE; GENE DUPLICATION; GENOME; HEREDITARY MOTOR AND SENSORY NEUROPATHIES; HUMANS; INTERSPERSED REPETITIVE SEQUENCES; MALE; MICE; MYELIN PROTEINS; PHYSICAL CHROMOSOME MAPPING; PSEUDOGENES; RECOMBINATION, GENETIC; SEQUENCE ANALYSIS, DNA; SULFOTRANSFERASES;

BACTERIA (MICROORGANISMS); PRIMATES;

EID: 0034830932     PISSN: 10889051     EISSN: None     Source Type: Journal    
DOI: 10.1101/gr.180401     Document Type: Article

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