SPTAN1 variants as a potential cause for autosomal...

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Journal of Human Genetics 2019 / 9

SPTAN1 variants as a potential cause for autosomal recessive hereditary spastic paraplegia

Leveille, Etienne, Estiar, Mehrdad A., Krohn, Lynne, Spiegelman, Dan, Dionne-Laporte, Alexandre, Dupré, Nicolas, Trempe, Jean François, Rouleau, Guy A., Gan-Or, Ziv
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Journal:
Journal of Human Genetics
DOI:
10.1038/s10038-019-0669-2
Date:
September, 2019
File:
PDF, 590 KB
2019
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