Results
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12041.
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12042.
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12043.
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12044.
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12045.
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12046.
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12047.
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A recessive form of central core disease, transiently presenting as multi-minicore disease, is associated with a homozygous mutation in the ryanodine receptor type 1 gene. [electronic resource] by
- Ferreiro, Ana
- Monnier, Nicole
- Romero, Norma B
- Leroy, Jean-Paul
- Bönnemann, Carsten
- Haenggeli, Charles-Antoine
- Straub, Volker
- Voss, Wolfgang D
- Nivoche, Yves
- Jungbluth, Heinz
- Lemainque, Arnaud
- Voit, Thomas
- Lunardi, Joël
- Fardeau, Michel
- Guicheney, Pascale
Producer: 20020809
In:
Annals of neurology vol. 51
Availability: No items available.
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12048.
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12049.
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Further evidence that SPG3A gene mutations cause autosomal dominant hereditary spastic paraplegia. [electronic resource] by
- Muglia, Maria
- Magariello, Angela
- Nicoletti, Giuseppe
- Patitucci, Alessandra
- Gabriele, Anna Lia
- Conforti, Francesca Luisa
- Mazzei, Rosalucia
- Caracciolo, Manuela
- Ardito, Bonaventura
- Lastilla, Marcello
- Tedeschi, Gioacchino
- Quattrone, Aldo
Producer: 20020809
In:
Annals of neurology vol. 51
Availability: No items available.
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12050.
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12051.
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12052.
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12053.
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12054.
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12055.
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12056.
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12057.
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12058.
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12059.
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12060.
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