Prenatal one-carbon metabolism dysregulation programs schizophrenia-like deficits
Alachkar, A, Wang, L, Yoshimura, R, Hamzeh, A R, Wang, Z, Sanathara, N, Lee, S M, Xu, X, Abbott, G W, Civelli, O
Published in Molecular psychiatry (01.02.2018)
Published in Molecular psychiatry (01.02.2018)
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Novel SPG20 mutation in an extended family with Troyer syndrome
Bizzari, S., Hamzeh, A. R., Nair, P., Mohamed, M., Saif, F., Aithala, G., Al-Ali, M. T., Bastaki, F.
Published in Metabolic brain disease (01.12.2017)
Published in Metabolic brain disease (01.12.2017)
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A novel missense mutation in ATRX uncovered in a Yemeni family leads to alpha-thalassemia/mental retardation syndrome without alpha-thalassemia
Hamzeh, A. R., Nair, P., Mohamed, M., Saif, F., Tawfiq, N., Al-Ali, M. T., Bastaki, F.
Published in Irish journal of medical science (01.05.2017)
Published in Irish journal of medical science (01.05.2017)
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Journal Article