SLC25A46 mutations underlie progressive myoclonic ataxia with optic atrophy and neuropathy

Gavin Charlesworth, Bettina Balint, Niccolò E. Mencacci, Lucinda Carr, Nicholas W. Wood, Kailash P. Bhatia*

*Corresponding author for this work

Research output: Contribution to journalLetter

10 Citations (Scopus)
Original languageEnglish (US)
Pages (from-to)1249-1251
Number of pages3
JournalMovement Disorders
Volume31
Issue number8
DOIs
StatePublished - Aug 1 2016

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Optic Atrophy
Optic Nerve Diseases
Ataxia
Mutation

ASJC Scopus subject areas

  • Neurology
  • Clinical Neurology

Cite this

Charlesworth, G., Balint, B., Mencacci, N. E., Carr, L., Wood, N. W., & Bhatia, K. P. (2016). SLC25A46 mutations underlie progressive myoclonic ataxia with optic atrophy and neuropathy. Movement Disorders, 31(8), 1249-1251. https://doi.org/10.1002/mds.26716
Charlesworth, Gavin ; Balint, Bettina ; Mencacci, Niccolò E. ; Carr, Lucinda ; Wood, Nicholas W. ; Bhatia, Kailash P. / SLC25A46 mutations underlie progressive myoclonic ataxia with optic atrophy and neuropathy. In: Movement Disorders. 2016 ; Vol. 31, No. 8. pp. 1249-1251.
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Charlesworth, G, Balint, B, Mencacci, NE, Carr, L, Wood, NW & Bhatia, KP 2016, 'SLC25A46 mutations underlie progressive myoclonic ataxia with optic atrophy and neuropathy', Movement Disorders, vol. 31, no. 8, pp. 1249-1251. https://doi.org/10.1002/mds.26716

SLC25A46 mutations underlie progressive myoclonic ataxia with optic atrophy and neuropathy. / Charlesworth, Gavin; Balint, Bettina; Mencacci, Niccolò E.; Carr, Lucinda; Wood, Nicholas W.; Bhatia, Kailash P.

In: Movement Disorders, Vol. 31, No. 8, 01.08.2016, p. 1249-1251.

Research output: Contribution to journalLetter

TY - JOUR

T1 - SLC25A46 mutations underlie progressive myoclonic ataxia with optic atrophy and neuropathy

AU - Charlesworth, Gavin

AU - Balint, Bettina

AU - Mencacci, Niccolò E.

AU - Carr, Lucinda

AU - Wood, Nicholas W.

AU - Bhatia, Kailash P.

PY - 2016/8/1

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DO - 10.1002/mds.26716

M3 - Letter

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SP - 1249

EP - 1251

JO - Movement Disorders

JF - Movement Disorders

SN - 0885-3185

IS - 8

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Charlesworth G, Balint B, Mencacci NE, Carr L, Wood NW, Bhatia KP. SLC25A46 mutations underlie progressive myoclonic ataxia with optic atrophy and neuropathy. Movement Disorders. 2016 Aug 1;31(8):1249-1251. https://doi.org/10.1002/mds.26716