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The SPTLC1 p.S331 mutation bridges sensory neuropathy and motor neuron disease and has implications for treatment.

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Title: The SPTLC1 p.S331 mutation bridges sensory neuropathy and motor neuron disease and has implications for treatment.
Authors: Fiorillo, Chiara1,2 (AUTHOR) chiara.fiorillo@edu.unige.it, Capodivento, Giovanna1,3 (AUTHOR), Geroldi, Alessandro1 (AUTHOR), Tozza, Stefano4 (AUTHOR), Moroni, Isabella5 (AUTHOR), Mohassel, Payam6 (AUTHOR), Cataldi, Matteo1,7 (AUTHOR), Campana, Chiara7 (AUTHOR), Morando, Simone8 (AUTHOR), Panicucci, Chiara8 (AUTHOR), Pedemonte, Marina2 (AUTHOR), Brolatti, Noemi2 (AUTHOR), Siliquini, Sabrina9 (AUTHOR), Traverso, Monica2 (AUTHOR), Baratto, Serena8 (AUTHOR), Debellis, Doriana10 (AUTHOR), Magri, Stefania11 (AUTHOR), Prada, Valeria12 (AUTHOR), Bellone, Emilia1,13 (AUTHOR), Salpietro, Vincenzo1,2 (AUTHOR)
Source: Neuropathology & Applied Neurobiology. Dec2022, Vol. 48 Issue 7, p1-15. 15p.
Database: Academic Search Ultimate
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  Data: The SPTLC1 p.S331 mutation bridges sensory neuropathy and motor neuron disease and has implications for treatment.
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  Data: <searchLink fieldCode="JN" term="%22Neuropathology+%26+Applied+Neurobiology%22">Neuropathology & Applied Neurobiology</searchLink>. Dec2022, Vol. 48 Issue 7, p1-15. 15p.
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