Researcher
Nigel Laing
University of Western Australia
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5 papers found
All papers authored by Nigel Laing
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2022
Igor Stevanovski 
,
Sanjog R. Chintalaphani ,
Hasindu Gamaarachchi ,
James M. Ferguson ,
Sandy S. Pineda ,
Carolin K. Scriba,
Michel Tchan ,
Victor Fung ,
Karl Ng ,
Andrea Cortese,
Henry Houlden ,
Carol Dobson-Stone ,
Lauren Fitzpatrick,
Glenda Halliday ,
Gianina Ravenscroft
and 6 other authors
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,
Sanjog R. Chintalaphani ,
Hasindu Gamaarachchi ,
James M. Ferguson ,
Sandy S. Pineda ,
Carolin K. Scriba,
Michel Tchan ,
Victor Fung ,
Karl Ng ,
Andrea Cortese,
Henry Houlden ,
Carol Dobson-Stone ,
Lauren Fitzpatrick,
Glenda Halliday ,
Gianina Ravenscroft
and 6 other authors
Download from doi.org
2020
Joshua S. Clayton,
Elyshia L. McNamara,
Hayley Goullee,
Stefan Conijn,
Keren Muthsam,
Gabrielle C. Musk,
David Coote,
James Kijas,
Alison C. Testa,
Rhonda L. Taylor,
Amanda J. O’Hara,
David Groth,
Coen Ottenheijm,
Gianina Ravenscroft ,
Nigel G. Laing
and 1 other authors
,
Nigel G. Laing
and 1 other authors
Ovine congenital progressive muscular dystrophy (OCPMD) is a model of TNNT1 congenital myopathy
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2018
Edith Bonnin,
Pauline Cabochette,
Alessandro Filosa ,
Ramona Jühlen ,
Shoko Komatsuzaki,
Mohammed Hezwani,
Achim Dickmanns,
Valérie Martinelli,
Marjorie Vermeersch,
Lynn Supply,
Nuno Martins ,
Laurence Pirenne ,
Gianina Ravenscroft ,
Marcus Lombard,
Sarah Port
and 11 other authors
,
Ramona Jühlen ,
Shoko Komatsuzaki,
Mohammed Hezwani,
Achim Dickmanns,
Valérie Martinelli,
Marjorie Vermeersch,
Lynn Supply,
Nuno Martins ,
Laurence Pirenne ,
Gianina Ravenscroft ,
Marcus Lombard,
Sarah Port
and 11 other authors
Biallelic mutations in nucleoporin NUP88 cause lethal fetal akinesia deformation sequence
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Gianina Ravenscroft ,
Robert J. Bryson-Richardson,
Kristen J. Nowak,
Nigel G. Laing
,
Robert J. Bryson-Richardson,
Kristen J. Nowak,
Nigel G. Laing
Recent advances in understanding congenital myopathies
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