Myosin storage myopathy associated with a heterozygous missense mutation in MYH7

Annals of Neurology

Volumn 54, Issue 4, 2003, Pages 494-500

  Tajsharghi, Homa ^a   Thornell, Lars Eric ^b   Lindberg, Christopher ^a   Lindvall, Björn ^c   Henriksson, Karl Gösta ^c   Oldfors, Anders ^a  

^a SAHLGRENSKA UNIVERSITY HOSPITAL   (Sweden)

^b UMEÅ UNIVERSITY   (Sweden)

^c LINKÖPING UNIVERSITY HOSPITAL   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

ISOPROTEIN; MYOSIN HEAVY CHAIN;

ADULT; AGED; ARTICLE; CASE REPORT; DISEASE COURSE; FAMILIAL HYPERTROPHIC CARDIOMYOPATHY; FEMALE; GENE; HEART MUSCLE; HUMAN; MALE; MISSENSE MUTATION; MUSCLE ATROPHY; MUSCLE CELL; MUSCLE WEAKNESS; MYH7 GENE; MYOFILAMENT; MYOPATHY; MYOSIN STORAGE MYOPATHY; NUCLEOTIDE SEQUENCE; ONSET AGE; PRIORITY JOURNAL; SKELETAL MUSCLE;

ADENOSINE TRIPHOSPHATASES; AGED; ARGININE; BLOTTING, WESTERN; DNA MUTATIONAL ANALYSIS; FAMILY HEALTH; FEMALE; HETEROZYGOTE; HUMANS; IMMUNOHISTOCHEMISTRY; MALE; MICROSCOPY, ELECTRON; MOLECULAR MOTOR PROTEINS; MOLECULAR SEQUENCE DATA; MUSCLE FIBERS, SLOW-TWITCH; MUSCULAR DISEASES; MUTATION, MISSENSE; MYOSIN HEAVY CHAINS; PROTEIN ISOFORMS; SEQUENCE ALIGNMENT; STAINING AND LABELING; TRYPTOPHAN;

EID: 0141535360     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.10693     Document Type: Article

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