Chen, Suqin, Zhou, Yan, Li, Xunhua, Labu, , Huang, Shuang, Huang, Weijun, Zhou, Chunlong, Maxwell, Patrick H., Wang, Yiming (2006) Genetic and structural analyses suggest that a novel SPG3A mutation causes severe phenotypes of hereditary spastic paraplegia. Chinese Science Bulletin, 51 (16). 2038-2040 doi:10.1007/s11434-006-2086-0
Reference Type | Journal (article/letter/editorial) | ||
---|---|---|---|
Title | Genetic and structural analyses suggest that a novel SPG3A mutation causes severe phenotypes of hereditary spastic paraplegia | ||
Journal | Chinese Science Bulletin | ||
Authors | Chen, Suqin | Author | |
Zhou, Yan | Author | ||
Li, Xunhua | Author | ||
Labu, | Author | ||
Huang, Shuang | Author | ||
Huang, Weijun | Author | ||
Zhou, Chunlong | Author | ||
Maxwell, Patrick H. | Author | ||
Wang, Yiming | Author | ||
Year | 2006 (August) | Volume | 51 |
Issue | 16 | ||
Publisher | Springer Science and Business Media LLC | ||
DOI | doi:10.1007/s11434-006-2086-0Search in ResearchGate | ||
Generate Citation Formats | |||
Mindat Ref. ID | 7102778 | Long-form Identifier | mindat:1:5:7102778:2 |
GUID | 0 | ||
Full Reference | Chen, Suqin, Zhou, Yan, Li, Xunhua, Labu, , Huang, Shuang, Huang, Weijun, Zhou, Chunlong, Maxwell, Patrick H., Wang, Yiming (2006) Genetic and structural analyses suggest that a novel SPG3A mutation causes severe phenotypes of hereditary spastic paraplegia. Chinese Science Bulletin, 51 (16). 2038-2040 doi:10.1007/s11434-006-2086-0 | ||
Plain Text | Chen, Suqin, Zhou, Yan, Li, Xunhua, Labu, , Huang, Shuang, Huang, Weijun, Zhou, Chunlong, Maxwell, Patrick H., Wang, Yiming (2006) Genetic and structural analyses suggest that a novel SPG3A mutation causes severe phenotypes of hereditary spastic paraplegia. Chinese Science Bulletin, 51 (16). 2038-2040 doi:10.1007/s11434-006-2086-0 | ||
In | (2006, August) Chinese Science Bulletin Vol. 51 (16) Springer Science and Business Media LLC |
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