P5.46 LPIN1 gene mutations can cause familial rhabdomyolysis and unexpected death in infancy
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| Veröffentlicht in: | Neuromuscular disorders : NMD 2011-10, Vol.21 (9), p.738-738 |
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| container_end_page | 738 |
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| container_issue | 9 |
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| container_title | Neuromuscular disorders : NMD |
| container_volume | 21 |
| creator | von der Hagen, M Smitka, M Michot, C Hubert, L de Kevzer, Y Huebner, A de Lonlay, P |
| description | |
| doi_str_mv | 10.1016/j.nmd.2011.06.1075 |
| format | Article |
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| fulltext | fulltext |
| identifier | ISSN: 0960-8966 |
| ispartof | Neuromuscular disorders : NMD, 2011-10, Vol.21 (9), p.738-738 |
| issn | 0960-8966 1873-2364 |
| language | eng |
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| source | Elsevier ScienceDirect Journals |
| subjects | Neurology |
| title | P5.46 LPIN1 gene mutations can cause familial rhabdomyolysis and unexpected death in infancy |
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