Dominant GDAP1 mutations cause predominantly mild CMT phenotypes - Research Collection

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Author

Date

2011-08

Type

Journal Article

ETH Bibliography

yes

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Publication status

published

External links

https://doi.org/10.1212/WNL.0b013e318228fc70

Journal / series

Neurology

Volume

77(6)

Pages / Article No.

540 - 548

Publisher

Lippincott Williams & Wilkins

Organisational unit

03367 - Suter, Ulrich / Suter, Ulrich

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ETH Bibliography

yes

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