E. M. Malik

Single‐center experience of N‐linked Congenital Disorders of Glycosylation with a Summary of Molecularly Characterized Cases in Arabs

F. Bastaki, S. Bizzari, S. Hamici, 2018, Annals of human genetics.

yearsoldchildrenwithsorethroatasclinicalindicatorsofGASpharyngitis.However,weneedtohavea lowthresholdtogiveantibioticstopatientswithsorethroatlivinginareasendemicforRHD.

E. M. Malik, Sulafa K M Ali, 2014 .

Erratum to: Novel ECHS1 mutation in an Emirati neonate with severe metabolic acidosis

F. Bastaki, P. Nair, M. Mohamed, 2016, Metabolic Brain Disease.

Identification of a novel CTCF mutation responsible for syndromic intellectual disability – a case report

F. Bastaki, P. Nair, M. Mohamed, 2017, BMC Medical Genetics.

Novel PDE6A mutation in an Emirati patient with retinitis pigmentosa

F. Bastaki, P. Nair, E. M. Malik, 2017, Oman journal of ophthalmology.

Novel ECHS1 mutation in an Emirati neonate with severe metabolic acidosis

F. Bastaki, P. Nair, M. Mohamed, 2016, Metabolic Brain Disease.