Familial inclusion body myositis: Evidence for autosomal dominant inheritance

Neurology

Volumn 42, Issue 4, 1992, Pages 897-902

  Neville, Hans E ^a,b   Baumbach, L L ^c   Ringel, S P ^a   Russo, L S ^d   Sujansky, E ^a   Garcia, C A ^e  

^a UNIVERSITY OF COLORADO SCHOOL OF MEDICINE   (United States)

^b VETERANS AFFAIRS MEDICAL CENTER   (United States)

^c UNIVERSITY OF MIAMI MILLER SCHOOL OF MEDICINE   (United States)

^d UNIVERSITY OF FLORIDA HEALTH SCIENCE CENTER   (United States)

^e LOUISIANA STATE UNIV MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ARTICLE; BIOPSY; CASE REPORT; CELL INCLUSION; CYTOCHEMISTRY; DOMINANT GENE; ELECTRON MICROSCOPY; FEMALE; GENETICS; HUMAN; MALE; METABOLISM; MUSCLE; MYOSITIS; PATHOLOGY; ULTRASTRUCTURE; AUTOSOMAL DOMINANT INHERITANCE; AUTOSOMAL RECESSIVE DISORDER; CHROMOSOME ANALYSIS; CLINICAL ARTICLE; CLINICAL FEATURE; DNA SEQUENCE; ELECTROMYOGRAM; GENE LOCUS; MUSCLE BIOPSY; PRIORITY JOURNAL; CONFERENCE PAPER; HISTOPATHOLOGY; HUMAN TISSUE;

ADULT; AGED; BIOPSY; CASE REPORT; FEMALE; GENES, DOMINANT; HISTOCYTOCHEMISTRY; HUMAN; INCLUSION BODIES; MALE; MICROSCOPY, ELECTRON; MIDDLE AGE; MUSCLES; MYOSITIS; SUPPORT, NON-U.S. GOV'T;

EID: 0026609582     PISSN: 00283878     EISSN: 1526632X     Source Type: Journal    
DOI: 10.1212/wnl.42.4.897     Document Type: Article

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