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A novel p.Gln175X [corrected] premature stop mutation in the C-terminal end of HSP27 is a cause of CMT2. [electronic resource] by
- Rossor, Alexander M
- Davidson, Gabrielle L
- Blake, Julian
- Polke, James M
- Murphy, Sinéad M
- Houlden, Henry
- Innes, Amy
- Kalmar, Bernadett
- Greensmith, Linda
- Reilly, Mary M
Producer: 20121029
In:
Journal of the peripheral nervous system : JPNS vol. 17
Availability: No items available.
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Charcot-Marie-Tooth disease: frequency of genetic subtypes and guidelines for genetic testing. [electronic resource] by
- Murphy, Sinead M
- Laura, Matilde
- Fawcett, Katherine
- Pandraud, Amelie
- Liu, Yo-Tsen
- Davidson, Gabrielle L
- Rossor, Alexander M
- Polke, James M
- Castleman, Victoria
- Manji, Hadi
- Lunn, Michael P T
- Bull, Karen
- Ramdharry, Gita
- Davis, Mary
- Blake, Julian C
- Houlden, Henry
- Reilly, Mary M
Producer: 20120816
In:
Journal of neurology, neurosurgery, and psychiatry vol. 83
Availability: No items available.
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