Molecular defects in the dysmyelinating mutant quaking

Journal of Neuroscience Research

Volumn 51, Issue 4, 1998, Pages 417-422

  Hardy, Rebecca J ^a,b  

^a UNIVERSITY OF EDINBURGH   (United Kingdom)

^b MOUNT SINAI MEDICAL CENTER   (United States)

Author keywords

KH domain; Myelination; Oligodendrocytes; qkI; RNA transport; Schwann cells

Indexed keywords

MESSENGER RNA; MYELIN; MYELIN ASSOCIATED GLYCOPROTEIN; MYELIN BASIC PROTEIN; MYELIN PROTEIN;

ANIMAL EXPERIMENT; ANIMAL MODEL; CHROMOSOME 17; CONTROLLED STUDY; DELETION MUTANT; GENE EXPRESSION; GENETIC DISORDER; MOUSE; MYELIN DEFICIENCY; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; SHORT SURVEY;

ANIMALS; DEMYELINATING DISEASES; GENES, RECESSIVE; MICE; MICE, QUAKING; MYELIN SHEATH; RNA-BINDING PROTEINS;

EID: 0032519750     PISSN: 03604012     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-4547(19980215)51:4<417::AID-JNR1>3.0.CO;2-F     Document Type: Short Survey

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