Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the δ-sarcoglycan gene

Nature Genetics

Volumn 14, Issue 2, 1996, Pages 195-198

  Nigro, V ^a   De Sa Moreira, E ^a   Piluso, G ^a   Vainzof, M ^a   Belsito, A ^a   Politano, L ^a   Puca, A A ^a   Passos Bueno, M R ^a   Zatz, M ^a  

^a UNIVERSITY OF SÃO PAULO   (Brazil)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; BRAZIL; CHROMOSOME 5Q; CLINICAL ARTICLE; FEMALE; FRAMESHIFT MUTATION; GENE DELETION; GENE LOCATION; HOMOZYGOSITY; HUMAN; LIMB GIRDLE MUSCULAR DYSTROPHY; MALE; PATHOGENESIS; PEDIGREE ANALYSIS; PRIORITY JOURNAL; RISK ASSESSMENT;

ADOLESCENT; ADULT; BRAZIL; CHILD; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 5; CYTOSKELETAL PROTEINS; DNA MUTATIONAL ANALYSIS; DNA, COMPLEMENTARY; DYSTROPHIN; FEMALE; FRAMESHIFT MUTATION; GENES, RECESSIVE; HOMOZYGOTE; HUMANS; MALE; MEMBRANE GLYCOPROTEINS; MOLECULAR SEQUENCE DATA; MUSCLE, SKELETAL; MUSCULAR DYSTROPHIES; PELVIS; SARCOGLYCANS; SARCOLEMMA; SHOULDER;

EID: 0029816797     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng1096-195     Document Type: Article

References (0)