Shumaila Zulfiqar

A missense variant in ITPR1 provides evidence for autosomal recessive SCA29 with asymptomatic cerebellar hypoplasia in carriers

Joakim Klar, Zafar Ali, Muhammad Farooq et al. · European Journal of Human Genetics · 2017 · 29 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Homozygous GRID2 missense mutation predicts a shift in the D-serine binding domain of GluD2 in a case with generalized brain atrophy and unusual clinical features

Zafar Ali, Shumaila Zulfiqar, Joakim Klar et al. · BMC Medical Genetics · 2017 · 28 citations · Full text

Life Sciences, Genetics, Neurology +17

Whole exome sequencing identifies novel variant underlying hereditary spastic paraplegia in consanguineous Pakistani families

Shumaila Zulfiqar, Muhammad Tariq, Zafar Ali et al. · Journal of Clinical Neuroscience · 2019 · 14 citations

Life Sciences, Genetics, Molecular Genetics +9