Hereditary cerebellar ataxia with Leber's hereditary optic neuropathy mitochondrial DNA 11778 mutation-Reference-Cited by-同舟云学术

Hereditary cerebellar ataxia with Leber's hereditary optic neuropathy mitochondrial DNA 11778 mutation

Published:1996-10 Issue:1-2 Volume:142 Page:111-113
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Murakami Tatsufumi,Mita Shuji,Tokunaga Makoto,Maeda Hiroko,Ueyama Hidetsugu,Kumamoto Toshihide,Uchino Makoto,Ando Masayuki

Publisher

Elsevier BV

Subject

Clinical Neurology,Neurology

Reference17 articles.

1. Neurological studies in families with Leber's optic atrophy;de Weerdt;Acta Neurol. Scandinav.,1971

2. Eadie, M.J. (1991) Cerebello-olivary atrophy. In: Vinken, P.J., Bruyn, G.B., Klawans, H.L. and de Jong, J.M.B.V. (Eds.). Handbook of Clinical Neurology, Vol. 16, Elsevier Science Publishers. Amsterdam, pp. 569–573.

3. Leber's optic atrophy and its relationship with the heredo-familial ataxias;Ferguson;J. Neurol. Psychopathol.,1928

4. Association of the 11778 mitochondrial DNA mutation and demyelinating disease;Flanigan;Neurology,1993

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