Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping-Reference-Cited by-同舟云学术

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

Published:1993-10 Issue:2 Volume:5 Page:195-200
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

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

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng1093-195.pdf

Reference33 articles.

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2. Burck, U., Goebel, H.H., Kuhlendahl, H.D., Meier, C. & Goebel, K.M. Neuromyopathy and vitamin E deficiency in man. Neuropediatrics 12, 267–278 (1981).

3. Harding, A.E. et al. Spinocerebellar degeneration associated with a selective defect of vitamin E absorption. New Engl. J. Med. 313, 32–35 (1985).

4. Krendel, D.A., Gilchrist, J.M., Johnson, A.O. & Bossen, E.H. Isolated deficiency of vitamin E with progressive neurologic deterioration. Neurology 37, 538–540 (1987).

5. Yokota, T. et al. Adult-onset spinocerebellar syndrome with idiopathic vitamin E deficiency. Ann. Neurol. 22, 84–87 (1987).

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