Duchenne muscular dystrophy (DMD) gene cDNA 8 Pstl and Taql Polymorphisms involve exon 51 of the Hindlll 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), pp.4284-4284

1990

Details

Title: Duchenne muscular dystrophy (DMD) gene cDNA 8 Pstl and Taql Polymorphisms involve exon 51 of the Hindlll map
Authors/Creators: N.G. Laing - Queen Elizabeth II Medical Centre
P.A. Akkari - Queen Elizabeth II Medical Centre
D.C. Chandler - Queen Elizabeth II Medical Centre
H.E. Thomas - Queen Elizabeth II Medical Centre
M.G. Layton - Queen Elizabeth II Medical Centre
M.E. Mears - Queen Elizabeth II Medical Centre
B.A. Kakulas - Queen Elizabeth II Medical Centre
Publication Details: Nucleic acids research, Vol.18(14), pp.4284-4284
Publisher: OXFORD UNIV PRESS UNITED KINGDOM
Number of pages: 1
Identifiers: 991005616565407891
Copyright: © 1990 Oxford University Press
Murdoch Affiliation: Centre for Molecular Medicine and Innovative Therapeutics
Language: English
Resource Type: Journal article

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Collaboration types: Domestic collaboration
Citation topics: 1 Clinical & Life Sciences; 1.255 Musculoskeletal Disorders; 1.255.628 Duchenne Muscular Dystrophy
Web Of Science research areas: Biochemistry & Molecular Biology
ESI research areas: Biology & Biochemistry