G.P.1.03 King-Denborough syndrome associated with mutations...

G.P.1.03 King-Denborough syndrome associated with mutations in the skeletal muscle ryanodine receptor (RYR1) gene

J. Dowling, S. Lillis, K. Amburgey, S. Leber, H. Zhou, S. Al-Sarraj, E. Wraige, S. Abbs, C. Sewry, F. Muntoni, H. Jungbluth

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Volume:

Year:

2009

Language:

english

DOI:

10.1016/j.nmd.2009.06.045

File:

PDF, 54 KB

english, 2009

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