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

✍ Scribed by Ben Hamida, C.; Doerflinger, N.; Belal, S.; Linder, C.; Reutenauer, L.; Dib, C.; Gyapay, G.; Vignal, A.; Le Paslier, D.; Cohen, D.

• Book ID: 109918225
• Publisher: Nature Publishing Group
• Year: 1993
• Tongue: English
• Weight: 803 KB
• Volume: 5
• Category: Article
• ISSN: 1061-4036
• DOI: 10.1038/ng1093-195