Exclusion of the SCN28 gene as candidate for CMT4B

European Journal of Human Genetics

Volumn 6, Issue 6, 1998, Pages 629-634

  Bolino, Alessandra ^a,d   Seri, Marco ^b   Caroli, Francesco ^b   Eubanks, James ^c   Srinivasan, Jayashree ^c   Mandich, Paola ^a   Schenone, Angelo ^d   Quattrone, Aldo ^e,f   Romeo, Giovanni ^a,g   Catterall, William A ^c   Devoto, Marcella ^a,d,h  

^a UNIVERSITY OF GENOA   (Italy)

^b G GASLINI INSTITUTE   (Italy)

^c UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE   (United States)

^d UNIVERSITY OF GENOA   (Italy)

^e UNIVERSITY MEDITERRANEA OF REGGIO CALABRIA   (Italy)

^f CNR   (Italy)

^g INTERNATIONAL AGENCY FOR RESEARCH ON CANCER   (France)

^h ROCKEFELLER UNIVERSITY   (United States)

Author keywords

Genomic structure; Peripheral neuropathy; Physical mapping; Sodium channel

Indexed keywords

BRAIN PROTEIN; SODIUM CHANNEL; VOLTAGE GATED CHANNEL FORMING PROTEIN; DNA; NERVE PROTEIN; SCN2B PROTEIN, HUMAN;

ARTICLE; CHROMOSOME 11Q; EXON; GENE MAPPING; GENE MUTATION; GENE STRUCTURE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; HUMAN CELL; INTRON; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; CHROMOSOME 11; CHROMOSOME MAP; GENETICS; MOLECULAR GENETICS; OPEN READING FRAME;

BASE SEQUENCE; CHARCOT-MARIE-TOOTH DISEASE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 11; DNA; EXONS; HUMANS; INTRONS; MOLECULAR SEQUENCE DATA; NERVE TISSUE PROTEINS; OPEN READING FRAMES; SODIUM CHANNELS;

EID: 0032217188     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5200220     Document Type: Article

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