Pathological and genetic analysis of the degenerating muscle (dmu) mouse: A new allele of Scn8a

Human Molecular Genetics

Volumn 10, Issue 17, 2001, Pages 1819-1827

  De Repentigny, Yves ^a,b   Côté, Patrice D ^a,b   Pool, Madeline ^a,b   Bernier, Gilbert ^c   Girard, Sonia ^b   Vidal, Silvia M ^b   Kothary, Rashmi ^a,b  

^a OTTAWA HOSPITAL RESEARCH INSTITUTE   (Canada)

^b UNIVERSITY OF OTTAWA   (Canada)

^c MAISONNEUVE ROSEMONT HOSPITAL   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

CARRIER PROTEIN; MED PROTEIN; PROTEIN SUBUNIT; SODIUM CHANNEL; UNCLASSIFIED DRUG;

ALLELE; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; BIRTH; CARDIOMYOPATHY; CHROMOSOME 12Q; CHROMOSOME 15; CONTROLLED STUDY; DEATH; DISEASE ASSOCIATION; DISEASE COURSE; DOWN REGULATION; GENE LOCUS; GENE MAPPING; GENE MUTATION; GENE TRANSLOCATION; GENETIC ANALYSIS; GENETIC CODE; GENETIC COMPLEMENTATION; GENETIC LINKAGE; HEART MUSCLE; HEREDITARY SPINAL MUSCULAR ATROPHY; HISTOPATHOLOGY; HUMAN; LOCOMOTION; MOUSE; MUSCLE ATROPHY; MUSCLE WEAKNESS; MUTANT; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; SCIATIC NERVE; SKELETAL MUSCLE; ULTRASTRUCTURE;

ANIMALIA;

EID: 0035880491     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/10.17.1819     Document Type: Article

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