Seven autosomal recessive limb-girdle muscular dystrophies in the Brazilian population: From LGMD2A to LGMD2G

American Journal of Medical Genetics

Volumn 82, Issue 5, 1999, Pages 392-398

  Passos Bueno, Maria Rita ^a   Vainzof, Mariz ^a   Moreira, Eloisa S ^a   Zatz, Mayana ^a  

^a UNIVERSITY OF SÃO PAULO   (Brazil)

Author keywords

Autosomal recessive; Clinical characterization; Limb girdle muscular dystrophies; Relative proportions

Indexed keywords

CREATINE KINASE; MONOCLONAL ANTIBODY; SARCOGLYCAN;

ADOLESCENT; ADULT; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHILD; FEMALE; GENE EXPRESSION; GENE MAPPING; GENE MUTATION; GENETIC LINKAGE; HEREDITARY SPINAL MUSCULAR ATROPHY; HUMAN; LIMB GIRDLE MUSCULAR DYSTROPHY; MAJOR CLINICAL STUDY; MALE; MOLECULAR CLONING; MUSCULAR DYSTROPHY; PRIORITY JOURNAL;

ADOLESCENT; ADULT; AGE OF ONSET; BRAZIL; CALPAIN; CHILD; CHILD, PRESCHOOL; CREATINE KINASE; CYTOSKELETAL PROTEINS; DYSTROGLYCANS; FEMALE; GENOTYPE; HUMANS; ISOENZYMES; MALE; MEMBRANE GLYCOPROTEINS; MEMBRANE PROTEINS; MIDDLE AGED; MUSCLE PROTEINS; MUSCULAR DYSTROPHIES; MUTATION; MUTATION, MISSENSE; PEPTIDE FRAGMENTS; PHENOTYPE; SARCOGLYCANS;

EID: 0033582745     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19990219)82:5<392::AID-AJMG7>3.0.CO;2-0     Document Type: Article

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