Search Results - Abdul Murad, N.A.

A novel mutation in exon 5 of the low density lipoprotein receptor gene in a Malay family with familial hypercholesterolaemia (FH) by Abdul Murad N. A., Hapizah M. N., Khalid Y., Khalid BAK, Jamal R.

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DRD and GRIN2B polymorphisms and their association with the development of impulse control behaviour among Malaysian Parkinson’s disease patients by Zainal Abidin, S., Tan, E.L., Chan, S.C., Jaafar, Ameerah, Lee, A.X., Abd Hamid, M.H.N., Abdul Murad, N.A., Pakarul Razy, N.F., Azmin, S., Ahmad-Annuar, Azlina, Lim, Shen Yang, Cheah, P.S., Ling, K.H., Mohamed Ibrahim, N.

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Hb lepore/β0-thalassaemia with α+-thalassaemia interactions, a potential diagnostic pitfall by Alauddin H., Mohamad Nasir S., Ahadon M., Raja Sabudin R.Z.A., Ithnin A., Hussin N.H., Alias H., Loh C.-K., Abdul Latiff Z., Abdul Murad N.A., Othman A.

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