Novel loss of function mutations in Asian kindreds with hereditary spastic paraplegia and thin corpus callosurn (SPG11)
| Автори: | , , , , , , , |
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| Формат: | Conference item |
| Опубліковано: |
2007
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| _version_ | 1826281832137621504 |
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| author | Baumber, L Patel, S Kinning, E Critchley, P Nemeth, A Talbot, K Maher, E Trembath, R |
| author_facet | Baumber, L Patel, S Kinning, E Critchley, P Nemeth, A Talbot, K Maher, E Trembath, R |
| author_sort | Baumber, L |
| collection | OXFORD |
| description | |
| first_indexed | 2024-03-07T00:34:43Z |
| format | Conference item |
| id | oxford-uuid:8102e45c-85d3-4e45-bd38-233f472c3d6e |
| institution | University of Oxford |
| last_indexed | 2024-03-07T00:34:43Z |
| publishDate | 2007 |
| record_format | dspace |
| spelling | oxford-uuid:8102e45c-85d3-4e45-bd38-233f472c3d6e2022-03-26T21:27:22ZNovel loss of function mutations in Asian kindreds with hereditary spastic paraplegia and thin corpus callosurn (SPG11)Conference itemhttp://purl.org/coar/resource_type/c_5794uuid:8102e45c-85d3-4e45-bd38-233f472c3d6eSymplectic Elements at Oxford2007Baumber, LPatel, SKinning, ECritchley, PNemeth, ATalbot, KMaher, ETrembath, R |
| spellingShingle | Baumber, L Patel, S Kinning, E Critchley, P Nemeth, A Talbot, K Maher, E Trembath, R Novel loss of function mutations in Asian kindreds with hereditary spastic paraplegia and thin corpus callosurn (SPG11) |
| title | Novel loss of function mutations in Asian kindreds with hereditary spastic paraplegia and thin corpus callosurn (SPG11) |
| title_full | Novel loss of function mutations in Asian kindreds with hereditary spastic paraplegia and thin corpus callosurn (SPG11) |
| title_fullStr | Novel loss of function mutations in Asian kindreds with hereditary spastic paraplegia and thin corpus callosurn (SPG11) |
| title_full_unstemmed | Novel loss of function mutations in Asian kindreds with hereditary spastic paraplegia and thin corpus callosurn (SPG11) |
| title_short | Novel loss of function mutations in Asian kindreds with hereditary spastic paraplegia and thin corpus callosurn (SPG11) |
| title_sort | novel loss of function mutations in asian kindreds with hereditary spastic paraplegia and thin corpus callosurn spg11 |
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