Conference item
Novel loss of function mutations in Asian kindreds with hereditary spastic paraplegia and thin corpus callosurn (SPG11)
- Publication status:
- Published
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Bibliographic Details
- Volume:
- 44
- Pages:
- S82-S82
- Host title:
- JOURNAL OF MEDICAL GENETICS
- Publication date:
- 2007-09-01
- ISSN:
-
0022-2593
- Source identifiers:
-
346148
Item Description
- Pubs id:
-
pubs:346148
- UUID:
-
uuid:8102e45c-85d3-4e45-bd38-233f472c3d6e
- Local pid:
- pubs:346148
- Deposit date:
- 2012-12-19
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- Copyright date:
- 2007
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