Edg-2 in myelin-forming cells: Isoforms, genomic mapping, and exclusion in Charcot-Marie-Tooth disease

GLIA

Volumn 26, Issue 2, 1999, Pages 176-185

  Allard, Julien ^a   Barron, Sonia ^a   Trottier, Suzanne ^a   Cervera, Pascale ^b   Daumas Duport, Catherine ^b   Leguern, Eric ^c   Brice, Alexis ^c   Schwartz, Jean Charles ^a   Sokoloff, Pierre ^a  

^a CENTRE PAUL BROCA   (France)

^b Service d'Anatomopathologie   (France)

^c PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

Author keywords

Charcot Marie Tooth disease; Linkage study; Oligodendrocytes; Receptor isoforms

Indexed keywords

ALLELE; EXON; GENE MAPPING; GENETIC POLYMORPHISM; HEREDITARY MOTOR SENSORY NEUROPATHY; IN SITU HYBRIDIZATION; MUTATION;

EID: 0033119708     PISSN: 08941491     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1098-1136(199904)26:2<176::AID-GLIA8>3.0.CO;2-K     Document Type: Article

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