Dominantly inherited proximal myotonic myopathy and leucoencephalopathy in a family with an incidental CLCN1 mutation

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作者
Mastaglia, F
Harker, N
Phillips, B
Day, T
Hankey, G
Fabian, V
Laing, N
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[1] QUEEN ELIZABETH II MED CTR,AUSTRALIAN NEUROMUSCULAR RES INST,NEDLANDS,WA,AUSTRALIA
[2] ROYAL PERTH HOSP,DEPT NEUROPATHOL,PERTH,WA,AUSTRALIA
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R74 [神经病学与精神病学];
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页码:1120 / 1120
页数:1
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