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Late-onset axial myopathy with cores due to a novel dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene

Jungbluth, H; Lillis, S; Zhou, H; Abbs, S; Swash, M; Muntoni, F; (2008) Late-onset axial myopathy with cores due to a novel dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene. In: NEUROMUSCULAR DISORDERS. (pp. 809 - 809). PERGAMON-ELSEVIER SCIENCE LTD

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Type: Proceedings paper
Title: Late-onset axial myopathy with cores due to a novel dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene
Event: 13th International Congress of the World-Muscle-Society
Location: Newcastle upon Tyne, ENGLAND
Dates: 2008-09-29 - 2008-10-02
DOI: 10.1016/j.nmd.2008.06.292
UCL classification: UCL > Provost and Vice Provost Offices
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Pop Health Sciences > UCL GOS Institute of Child Health
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Pop Health Sciences > UCL GOS Institute of Child Health > ICH Developmental Neurosciences Prog
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Pop Health Sciences > UCL GOS Institute of Child Health > ICH Genetics and Genomic Medicine Prog
URI: http://discovery.ucl.ac.uk/id/eprint/66393
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