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Total truncation of the molybdopterin/dimerization domains of SUOX protein in an Arab family with isolated sulfite oxidase deficiency.
Am J Med Genet A. 2005 Jul 15;136(2):205-9. doi: 10.1002/ajmg.a.30796.
Am J Med Genet A. 2005.
PMID: 15952210
Preimplantation genetic diagnosis in isolated sulfite oxidase deficiency.
Salih MA, Bosley TM, Alorainy IA, Sabry MA, Rashed MS, Al-Yamani EA, El-Akoum S, Mohamed SH, Abu-Amero KK, Hellani AM.
Salih MA, et al.
Can J Neurol Sci. 2013 Jan;40(1):109-12. doi: 10.1017/s0317167100013081.
Can J Neurol Sci. 2013.
PMID: 23250141
No abstract available.
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Neurologic injury in isolated sulfite oxidase deficiency.
Bosley TM, Alorainy IA, Oystreck DT, Hellani AM, Seidahmed MZ, Osman Mel F, Sabry MA, Rashed MS, Al-Yamani EA, Abu-Amero KK, Salih MA.
Bosley TM, et al.
Can J Neurol Sci. 2014 Jan;41(1):42-8. doi: 10.1017/s0317167100016243.
Can J Neurol Sci. 2014.
PMID: 24384336
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Biotin-responsive basal ganglia disease maps to 2q36.3 and is due to mutations in SLC19A3.
Zeng WQ, Al-Yamani E, Acierno JS Jr, Slaugenhaupt S, Gillis T, MacDonald ME, Ozand PT, Gusella JF.
Zeng WQ, et al.
Am J Hum Genet. 2005 Jul;77(1):16-26. doi: 10.1086/431216. Epub 2005 May 3.
Am J Hum Genet. 2005.
PMID: 15871139
Free PMC article.
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