Filtry
Projekt
Autosomal recessive demyelinating neuropathy type CMT4C ? analysis of the SH3TC2 gene and a clinical study. (NT11521)
Defects in the SH3TC2 gene have been recently identified in patients with hereditary motor and sensory neuropathy (HMSN). Patients cohort of about 120 urelated individuals with the demyelinating hereditary neuropathy and pedigrees compatible with aut...
FH - Neurologie, neurochirurgie, neurovědy
- 2010 - 2013 •
- 3 846 tis. Kč •
- 3 846 tis. Kč •
- MZ
Řešení projektu: 1. 9. 2010 - 31. 12. 2013
Uznané náklady
Podpora ze státního rozpočtu (100%)
Poskytovatel: Ministerstvo zdravotnictví
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