Duchenne muscular dystrophy (DMD) gene cDNA 8 Pstl and Taql polymorphisms involve exon 51 of the hindIII map

Journal article

Peer reviewed

N. G Laing, P. A Akkari, D. C Chandler, H. E Thomas, M. G Layton, M. E Mears and B. A Kakulas

Nucleic acids research, Vol.18(14), p.4284

1990

Abstract

Biological and medical sciences

Diseases of striated muscles. Neuromuscular diseases

Medical sciences

Neurology

Title: Duchenne muscular dystrophy (DMD) gene cDNA 8 Pstl and Taql polymorphisms involve exon 51 of the hindIII map
Authors/Creators: N. G Laing - Australian neuromuscular res. inst., Queen Elizabeth II medical cent., Nedlands W. Aust. 6009, Australia
P. A Akkari - Australian neuromuscular res. inst., Queen Elizabeth II medical cent., Nedlands W. Aust. 6009, Australia
D. C Chandler - Australian neuromuscular res. inst., Queen Elizabeth II medical cent., Nedlands W. Aust. 6009, Australia
H. E Thomas - Australian neuromuscular res. inst., Queen Elizabeth II medical cent., Nedlands W. Aust. 6009, Australia
M. G Layton - Australian neuromuscular res. inst., Queen Elizabeth II medical cent., Nedlands W. Aust. 6009, Australia
M. E Mears - Australian neuromuscular res. inst., Queen Elizabeth II medical cent., Nedlands W. Aust. 6009, Australia
B. A Kakulas - Australian neuromuscular res. inst., Queen Elizabeth II medical cent., Nedlands W. Aust. 6009, Australia
Publication Details: Nucleic acids research, Vol.18(14), p.4284
Publisher: Oxford University Press
Identifiers: 991005616459307891
Murdoch Affiliation: Centre for Molecular Medicine and Innovative Therapeutics
Language: English
Resource Type: Journal article

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