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1978, Scripta series in mathematics, ISBN 9780470265406, 2v. --
Book
Chemistry letters, ISSN 0366-7022, 2017, Volume 46, Issue 2, pp. 154 - 162
Journal Article
2012, Springer series on atomic, optical, and plasma physics, ISBN 9781441981813, Volume 66, xvii, 308
Book
Revista de neurologiá, ISSN 0210-0010, 06/2008, Volume 46, Issue 11, pp. 684 - 692
Journal Article
Neurología (Barcelona, Spain), ISSN 0213-4853, 07/2015, Volume 30, Issue 6, pp. 347 - 351
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Rinshō shinkeigaku, ISSN 0009-918X, 2015, Volume 55, Issue 8, pp. 580 - 584
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Shengwu gongcheng xuebao, ISSN 1000-3061, 08/2015, Volume 31, Issue 8, p. 1247
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Zeitschrift für anorganische und allgemeine Chemie (1950), ISSN 0044-2313, 06/2008, Volume 634, Issue 6-7, pp. 1133 - 1139
Journal Article
Zhongguo zhongyao zazhi, ISSN 1001-5302, 05/2016, Volume 41, Issue 10, p. 1792
Journal Article
Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences, ISSN 1672-7347, 11/2012, Volume 37, Issue 11, p. 1183
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Eclética química, ISSN 0100-4670, 2007, Volume 32, Issue 2, pp. 7 - 11
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Chinese journal of preventive veterinary medicine, ISSN 1008-0589, 2011, Volume 33, Issue 8, pp. 661 - 664
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Nature reviews. Immunology, ISSN 1474-1733, 07/2009, Volume 9, Issue 7
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Bunseki kagaku, ISSN 0525-1931, 2009, Volume 58, Issue 8, pp. 681 - 686
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Anales de pediatría (Barcelona, Spain : 2003), ISSN 1695-4033, 04/2016, Volume 84, Issue 4, pp. 195 - 202
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Der Schmerz, ISSN 0932-433X, 6/2006, Volume 20, Issue 3, pp. 181 - 188
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Biochemistry (Easton), ISSN 0006-2960, 2007, Volume 46, Issue 12, pp. 3846 - 3855
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Revista brasileira de farmacognosia, ISSN 0102-695X, 01/2009, Volume 19, Issue 1 A, pp. 68 - 76
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Sheng li hsüeh pao, ISSN 0371-0874, 02/2020, Volume 72, Issue 1, p. 84
Journal Article
Revista de neurologiá, ISSN 0210-0010, 04/2019, Volume 68, Issue 7, pp. 312 - 314
Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Blepharoptosis - genetics | Humans | Wolff-Parkinson-White Syndrome - genetics | Mitochondrial Proteins - physiology | Fetal Growth Retardation - genetics | Infant | Male | Mitochondrial Proteins - genetics | Mutation, Missense | Leigh Disease - genetics | Disease Progression | Genetic Heterogeneity | Intellectual Disability - genetics | Point Mutation | Phenotype | DNA, Mitochondrial - genetics | Gastrointestinal Diseases - genetics | Electron Transport Complex I - genetics | Female | Electron Transport Complex I - physiology | Ophthalmoplegia - genetics
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