Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping

C. B. Hamida, N. Doerflinger, S. Belal, C. Linder, L. Reutenauer, C. Dib, G. Gyapay, A. Vignal, D. Le Paslier, D. Cohen, M. Pandolfo, V. Mokini, G. Novelli, F. Hentati, M. B. Hamida, J. L. Mandel, M. Koenig

Research output: Contribution to journalArticlepeer-review

Fingerprint Dive into the research topics of 'Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping'. Together they form a unique fingerprint.

Medicine & Life Sciences