Subclinical leukodystrophy and infertility in a man with a novel homozygous CLCN2 mutation

Daniela Di Bella; Davide Pareyson; Mario Savoiardo; Laura Farina; Claudia Ciano; Serena Caldarazzo; Anna Sagnelli; Sara Bonato; Simone Nava; Nereo Bresolin; Gioacchino Tedeschi; Franco Taroni; Ettore Salsano

doi:10.1212/WNL.0000000000000812

Subclinical leukodystrophy and infertility in a man with a novel homozygous CLCN2 mutation

Daniela Di Bella, Davide Pareyson, Mario Savoiardo, Laura Farina, Claudia Ciano, Serena Caldarazzo, Anna Sagnelli, Sara Bonato, Simone Nava, Nereo Bresolin, Gioacchino Tedeschi, Franco Taroni, Ettore Salsano

Research output: Contribution to journal › Article › peer-review

Original language	English
Pages (from-to)	1217-1218
Number of pages	2
Journal	Neurology
Volume	83
Issue number	13
DOIs	https://doi.org/10.1212/WNL.0000000000000812
Publication status	Published - Sept 1 2014

ASJC Scopus subject areas

Clinical Neurology
Medicine(all)

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10.1212/WNL.0000000000000812

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title = "Subclinical leukodystrophy and infertility in a man with a novel homozygous CLCN2 mutation",

author = "{Di Bella}, Daniela and Davide Pareyson and Mario Savoiardo and Laura Farina and Claudia Ciano and Serena Caldarazzo and Anna Sagnelli and Sara Bonato and Simone Nava and Nereo Bresolin and Gioacchino Tedeschi and Franco Taroni and Ettore Salsano",

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T1 - Subclinical leukodystrophy and infertility in a man with a novel homozygous CLCN2 mutation

AU - Di Bella, Daniela

AU - Pareyson, Davide

AU - Savoiardo, Mario

AU - Farina, Laura

AU - Ciano, Claudia

AU - Caldarazzo, Serena

AU - Sagnelli, Anna

AU - Bonato, Sara

AU - Nava, Simone

AU - Bresolin, Nereo

AU - Tedeschi, Gioacchino

AU - Taroni, Franco

AU - Salsano, Ettore

PY - 2014/9/1

Y1 - 2014/9/1

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U2 - 10.1212/WNL.0000000000000812

DO - 10.1212/WNL.0000000000000812

M3 - Article

C2 - 25128180

AN - SCOPUS:84921746317

SN - 0028-3878

VL - 83

SP - 1217

EP - 1218

JO - Neurology

JF - Neurology

IS - 13

ER -

Subclinical leukodystrophy and infertility in a man with a novel homozygous CLCN2 mutation

ASJC Scopus subject areas

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