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Muhammad Yasir Zahoor

University of the Punjab

3

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151

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Missense variants in AIMP1 gene are implicated in autosomal recessive intellectual disability without neurodegeneration

2016 European Journal of Human Genetics
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A compound heterozygous mutation in DPAGT1 results in a congenital disorder of glycosylation with a relatively mild phenotype

2013 European Journal of Human Genetics
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Homozygous and heterozygous disruptions of ANK3: at the crossroads of neurodevelopmental and psychiatric disorders

2013 Human Molecular Genetics
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