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Mitochondrial Dysfunction in a Patient with 8q21.11 Deletion and Charcot-Marie-Tooth Disease Type 2K due to GDAP1 Haploinsufficiency.
Mol Syndromol. 2015 Oct;6(4):204-6. doi: 10.1159/000440660. Epub 2015 Sep 18.
Mol Syndromol. 2015.
PMID: 26648837
Free PMC article.
Sjögren-Larsson syndrome: inherited defect in the fatty alcohol cycle.
Rizzo WB, Dammann AL, Craft DA, Black SH, Tilton AH, Africk D, Chaves-Carballo E, Holmgren G, Jagell S.
Rizzo WB, et al. Among authors: africk d.
J Pediatr. 1989 Aug;115(2):228-34. doi: 10.1016/s0022-3476(89)80070-8.
J Pediatr. 1989.
PMID: 2666627
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Transient neonatal hyperglycinemia.
Schiffmann R, Kaye EM, Willis JK 3rd, Africk D, Ampola M.
Schiffmann R, et al. Among authors: africk d.
Ann Neurol. 1989 Feb;25(2):201-3. doi: 10.1002/ana.410250218.
Ann Neurol. 1989.
PMID: 2919871
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The importance of recognizing secondary carnitine deficiency in organic acidaemias: case report in glutaric acidaemia type II.
Mandel H, Africk D, Blitzer M, Shapira E.
Mandel H, et al. Among authors: africk d.
J Inherit Metab Dis. 1988;11(4):397-402. doi: 10.1007/BF01800428.
J Inherit Metab Dis. 1988.
PMID: 2468819
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