Limb-girdle muscular dystrophy type 2H associated with mutation in TRIM32, a putative E3-ubiquitin-ligase gene

American Journal of Human Genetics

Volumn 70, Issue 3, 2002, Pages 663-672

  Frosk, Patrick ^a   Weiler, Tracey ^a   Nylen, Edward ^a   Sudha, Thangirala ^a   Greenberg, Cheryl R ^a   Morgan, Kenneth ^b   Fujiwara, T Mary ^b   Wrogemann, Klaus ^a  

^a UNIVERSITY OF MANITOBA   (Canada)

^b RESEARCH INSTITUTE OF THE MCGILL UNIVERSITY HEALTH CENTRE   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ASPARAGINE; ASPARTIC ACID; LIGASE; UBIQUITIN;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CANADA; CHROMOSOME 9Q; CLINICAL ARTICLE; DISEASE ASSOCIATION; EXON; FAMILY STUDY; GENBANK; GENE; GENE FUNCTION; GENE MUTATION; GENE TRIM32; GENETIC CODE; HAPLOTYPE; HOMOZYGOSITY; HUMAN; LIMB GIRDLE MUSCULAR DYSTROPHY; MICROSATELLITE MARKER; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN MOTIF; PROTEIN PROTEIN INTERACTION; PROTEIN STRUCTURE; SEQUENCE ANALYSIS;

EID: 0036179479     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/339083     Document Type: Article

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