Connatal Pelizaeus-Merzbacher disease associated with the jimpy(MSD) mice mutation

Pediatric Neurology

Volumn 20, Issue 4, 1999, Pages 309-311

  Komaki, Hirofumi ^a   Sasaki, Masayuki ^a   Yamamoto, Toshiyuki ^b   Iai, Mizue ^c   Takashima, Sachio ^c  

^a Dept Child Neurol Natl Ctr H   (Japan)

^b TOTTORI UNIVERSITY   (Japan)

^c NATIONAL INSTITUTE OF NEUROSCIENCE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

MYELIN; MYELIN BASIC PROTEIN; PROTEOLIPID PROTEIN;

ANIMAL MODEL; ARTICLE; CASE REPORT; GENE MUTATION; HUMAN; IMMUNOHISTOCHEMISTRY; INFANT; MALE; MOUSE; MYELIN DEFICIENCY; NONHUMAN; PELIZAEUS MERZBACHER DISEASE; PRIORITY JOURNAL; PROTEIN DEFICIENCY; PROTEIN EXPRESSION;

ANIMALS; BRAIN; DIFFUSE CEREBRAL SCLEROSIS OF SCHILDER; DISEASE MODELS, ANIMAL; FATAL OUTCOME; HUMANS; IMMUNOHISTOCHEMISTRY; INFANT; MALE; MICE; MICE, JIMPY; MYELIN PROTEOLIPID PROTEIN; POINT MUTATION;

EID: 0032905907     PISSN: 08878994     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0887-8994(98)00160-X     Document Type: Article

References (13)

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