Results
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89261.
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Classical infantile spinal muscular atrophy with SMN deficiency causes sensory neuronopathy. [electronic resource] by
- Rudnik-Schöneborn, S
- Goebel, H H
- Schlote, W
- Molaian, S
- Omran, H
- Ketelsen, U
- Korinthenberg, R
- Wenzel, D
- Lauffer, H
- Kreiss-Nachtsheim, M
- Wirth, B
- Zerres, K
Producer: 20040112
In:
Neurology vol. 60
Availability: No items available.
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89262.
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89263.
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89264.
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89265.
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89266.
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89267.
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89268.
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89269.
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89270.
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89271.
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89272.
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89273.
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89274.
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89275.
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89276.
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Identification and functional characterization of a novel R621C mutation in the synphilin-1 gene in Parkinson's disease. [electronic resource] by
- Marx, Frank P
- Holzmann, Carsten
- Strauss, Karsten M
- Li, Lei
- Eberhardt, Olaf
- Gerhardt, Ellen
- Cookson, Mark R
- Hernandez, Dena
- Farrer, Matt J
- Kachergus, Jennifer
- Engelender, Simone
- Ross, Christopher A
- Berger, Klaus
- Schöls, Ludger
- Schulz, Jörg B
- Riess, Olaf
- Krüger, Rejko
Producer: 20040130
In:
Human molecular genetics vol. 12
Availability: No items available.
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89277.
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89278.
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89279.
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89280.
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