Alexander disease causing hereditary late-onset ataxia with only minimal white matter changes: A report of two sibs

C.C.S. Delnooz, J.H. Schelhaas, B.P.C. van de Warrenburg, R.J. de Graaf, G.S. Salomons

Research output: Contribution to journalArticleAcademicpeer-review

Original languageUndefined/Unknown
Pages (from-to)1613-1615
JournalMovement Disorders
Volume23
Issue number11
DOIs
Publication statusPublished - 2008

Cite this

Delnooz, C.C.S. ; Schelhaas, J.H. ; van de Warrenburg, B.P.C. ; de Graaf, R.J. ; Salomons, G.S. / Alexander disease causing hereditary late-onset ataxia with only minimal white matter changes: A report of two sibs. In: Movement Disorders. 2008 ; Vol. 23, No. 11. pp. 1613-1615.
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title = "Alexander disease causing hereditary late-onset ataxia with only minimal white matter changes: A report of two sibs",
author = "C.C.S. Delnooz and J.H. Schelhaas and {van de Warrenburg}, B.P.C. and {de Graaf}, R.J. and G.S. Salomons",
year = "2008",
doi = "10.1002/mds.22053",
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volume = "23",
pages = "1613--1615",
journal = "Movement Disorders",
issn = "0885-3185",
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Alexander disease causing hereditary late-onset ataxia with only minimal white matter changes: A report of two sibs. / Delnooz, C.C.S.; Schelhaas, J.H.; van de Warrenburg, B.P.C.; de Graaf, R.J.; Salomons, G.S.

In: Movement Disorders, Vol. 23, No. 11, 2008, p. 1613-1615.

Research output: Contribution to journalArticleAcademicpeer-review

TY - JOUR

T1 - Alexander disease causing hereditary late-onset ataxia with only minimal white matter changes: A report of two sibs

AU - Delnooz, C.C.S.

AU - Schelhaas, J.H.

AU - van de Warrenburg, B.P.C.

AU - de Graaf, R.J.

AU - Salomons, G.S.

PY - 2008

Y1 - 2008

U2 - 10.1002/mds.22053

DO - 10.1002/mds.22053

M3 - Article

VL - 23

SP - 1613

EP - 1615

JO - Movement Disorders

JF - Movement Disorders

SN - 0885-3185

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ER -