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Familial encephalopathy and L-2-hydroxyglutaric aciduria.
Kaabachi N, Larnaout A, Rabier D, Jakobs C, Belal S, Hentati F, Parvey P, Bardet J, Ben Hamida M, Mebazaa A, et al. Kaabachi N, et al. Among authors: belal s. J Inherit Metab Dis. 1993;16(5):893. doi: 10.1007/BF00714285. J Inherit Metab Dis. 1993. PMID: 8295407 No abstract available.
Homozygosity mapping of giant axonal neuropathy gene to chromosome 16q24.1.
Ben Hamida C, Cavalier L, Belal S, Sanhaji H, Nadal N, Barhoumi C, M'Rissa N, Marzouki N, Mandel JL, Ben Hamida M, Koenig M, Hentati F. Ben Hamida C, et al. Among authors: belal s. Neurogenetics. 1997 Sep;1(2):129-33. doi: 10.1007/s100480050019. Neurogenetics. 1997. PMID: 10732815
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