Search Results - "IONANNOU, P"

Friedreich's ataxia phenotype not linked to chromosome 9 and associated with selective autosomal recessive vitamin E deficiency in two inbred Tunisian families by Ben Hamida, M, Belal, S, Sirugo, G, Ben Hamida, C, Panayides, K, Ionannou, P, Beckmann, J, Mandel, J L, Hentati, F, Koenig, M

“…Friedreich's ataxia (FA) is an autosomal recessive neurodegenerative disorder, the disease locus (FRDA) of which has been assigned to 9q13-q21.1 by genetic…”
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Friedrich's ataxia phenotype not linked to chromosome 9 and associated with selective autosomal recessive vitamin E deficiency in two inbred Tunisian families by BEN HAMIDA, M, BELAL, S, MIDDLETON, L, SIRUGO, G, BEN HAMIDA, C, PANAYIDES, K, IONANNOU, P, BECKMANN, J, MANDEL, J. L, HENTATI, F, KOENIG, M

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