A systematic comparison of all mutations in hereditary sensory neuropathy type I (HSAN I) reveals that the G387A mutation is not disease associated

T. Hornemann; A. Penno; S. Richard; G. Nicholson; F.S. van Dijk; A. Rotthier; V. Timmerman; A. von Eckardstein

doi:10.1007/s10048-008-0168-7

A systematic comparison of all mutations in hereditary sensory neuropathy type I (HSAN I) reveals that the G387A mutation is not disease associated

T. Hornemann, A. Penno, S. Richard, G. Nicholson, F.S. van Dijk, A. Rotthier, V. Timmerman, A. von Eckardstein

Research output: Contribution to journal › Article › Academic › peer-review

Original language	Undefined/Unknown
Pages (from-to)	135-143
Journal	Neurogenetics
Volume	10
Issue number	2
DOIs	https://doi.org/10.1007/s10048-008-0168-7
Publication status	Published - 2009

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10.1007/s10048-008-0168-7

http://www.springerlink.com/content/j7234808q63v4473/

Cite this

Hornemann, T., Penno, A., Richard, S., Nicholson, G., van Dijk, F. S., Rotthier, A., ... von Eckardstein, A. (2009). A systematic comparison of all mutations in hereditary sensory neuropathy type I (HSAN I) reveals that the G387A mutation is not disease associated. Neurogenetics, 10(2), 135-143. https://doi.org/10.1007/s10048-008-0168-7

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A systematic comparison of all mutations in hereditary sensory neuropathy type I (HSAN I) reveals that the G387A mutation is not disease associated. / Hornemann, T.; Penno, A.; Richard, S.; Nicholson, G.; van Dijk, F.S.; Rotthier, A.; Timmerman, V.; von Eckardstein, A.

In: Neurogenetics, Vol. 10, No. 2, 2009, p. 135-143.

Research output: Contribution to journal › Article › Academic › peer-review

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AU - Penno, A.

AU - Richard, S.

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AU - van Dijk, F.S.

AU - Rotthier, A.

AU - Timmerman, V.

AU - von Eckardstein, A.

PY - 2009

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