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Publications by Michel Koenig
Homozygosity Mapping of Portuguese and Japanese Forms of Ataxia-Oculomotor Apraxia to 9p13, and Evidence for Genetic Heterogeneity
American Journal of Human Genetics
Genetics
Homozygosity Mapping of Spinocerebellar Ataxia With Cerebellar Atrophy and Peripheral Neuropathy to 9q33–34, and With Hearing Impairment and Optic Atrophy to 6p21–23
European Journal of Human Genetics
Genetics