Identification of Alu elements mediating a partial PMP22 deletion

Neurogenetics

Volumn 7, Issue 2, 2006, Pages 119-126

  Matejas, Verena ^a   Huehne, Kathrin ^a   Thiel, Christian ^a   Sommer, Claudia ^b   Jakubiczka, Sibylle ^c   Rautenstrauss, Bernd ^a  

^a UNIVERSITY OF ERLANGEN NUREMBERG   (Germany)

^b UNIVERSITY OF WÜRZBURG   (Germany)

^c OTTO VON GUERICKE UNIVERSITY   (Germany)

Author keywords

CMT; HNPP; Partial deletion; PMP22

Indexed keywords

GENE PRODUCT; PERIPHERAL MYELIN PROTEIN 22; PRIMER DNA;

ADULT; ALU SEQUENCE; ARTICLE; BIOINFORMATICS; CASE REPORT; CHI LIKE SEQUENCE; CHROMOSOME 17P; CHROMOSOME BREAKAGE; CHROMOSOME DELETION; CONTROLLED STUDY; DIAGNOSTIC ERROR; DNA PROBE; DNA SEQUENCE; EXON; GENE; GENE AMPLIFICATION; GENE DELETION; GENETIC RECOMBINATION; HEREDITARY NEUROPATHY WITH LIABLITY TO PRESSURE PALSIES; HETEROZYGOSITY; HUMAN; HUMAN TISSUE; LOW COPY REPEAT; MALE; MULTIPLEX LIGATION DEPENDENT PROBE AMPLIFICATION; NEUROPATHY; NON ALLELIC HOMOLOGOUS RECOMBINATION; NUCLEOTIDE REPEAT; NUCLEOTIDE SEQUENCE; PMP22 GENE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM; TANDEM REPEAT;

ALU ELEMENTS; BASE SEQUENCE; DNA MUTATIONAL ANALYSIS; EXONS; GENE DELETION; HEREDITARY MOTOR AND SENSORY NEUROPATHIES; HEREDITARY SENSORY AND MOTOR NEUROPATHY; HUMANS; MALE; MIDDLE AGED; MOLECULAR SEQUENCE DATA; MYELIN PROTEINS;

EID: 33646422492     PISSN: 13646745     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10048-006-0030-8     Document Type: Article

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