Autosomal recessive axonal neuropathy caused by HINT1 mutation: New association of a psychiatric disorder to the neurologic phenotype

Gaia Scarpini; Carlotta Spagnoli; Grazia Gabriella Salerno; Susanna Rizzi; Daniele Frattini; Carlo Fusco

doi:10.1016/j.nmd.2019.05.001

Autosomal recessive axonal neuropathy caused by HINT1 mutation: New association of a psychiatric disorder to the neurologic phenotype

Gaia Scarpini, Carlotta Spagnoli, Grazia Gabriella Salerno, Susanna Rizzi, Daniele Frattini, Carlo Fusco

Research output: Contribution to journal › Letter

Original language	English
Number of pages	1
Journal	Neuromuscular Disorders
Volume	29
Issue number	12
DOIs	https://doi.org/10.1016/j.nmd.2019.05.001
Publication status	Published - Dec 2019

Keywords

HINT1
Mood disorder
Neuromyotonia
Neuropathy

ASJC Scopus subject areas

Pediatrics, Perinatology, and Child Health
Neurology
Clinical Neurology
Genetics(clinical)

Cite this

Scarpini, G., Spagnoli, C., Salerno, G. G., Rizzi, S., Frattini, D., & Fusco, C. (2019). Autosomal recessive axonal neuropathy caused by HINT1 mutation: New association of a psychiatric disorder to the neurologic phenotype. Neuromuscular Disorders, 29(12). https://doi.org/10.1016/j.nmd.2019.05.001

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author = "Gaia Scarpini and Carlotta Spagnoli and Salerno, {Grazia Gabriella} and Susanna Rizzi and Daniele Frattini and Carlo Fusco",

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AU - Rizzi, Susanna

AU - Frattini, Daniele

AU - Fusco, Carlo

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Access to Document

10.1016/j.nmd.2019.05.001