Hereditory Sensory Neuropathy Type 1 ( SPTLC1 ): phenotypic...

Neuromuscular Disorders 2017 / 03 Vol. 27

Hereditory Sensory Neuropathy Type 1 ( SPTLC1 ): phenotypic variation in patients with the English founder mutation

Kugathasan, U., Laurá, M., Tomaselli, P.J., Evans, M.R.B., Pittmann, A., Sinclair, C.J.D., Hornemann, T., Suriyanarayanan, S., Phadke, R., Lauria, G., Lombardi, R., Polke, J.M., Bennett, D.L., Houlden
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Volume:
27
Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/s0960-8966(17)30296-1
Date:
March, 2017
File:
PDF, 138 KB
english, 2017
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