Homozygous missense mutation in the LMAN2L gene segregates with intellectual disability in a large consanguineous Pakistani family

R Rafiullah, M Aslamkhan, N Paramasivam… - Journal of medical …, 2016 - jmg.bmj.com
Background Intellectual disability (ID) is a neurodevelopmental disorder affecting 1%–3% of
the population worldwide. It is characterised by high phenotypic and genetic heterogeneity …
被引用次数：20 相关文章

Homozygous missense mutation in the LMAN2L gene segregates with intellectual disability in a large consanguineous Pakistani family

R Rafiullah, M Aslamkhan, N Paramasivam… - Journal of Medical …, 2015 - jmg.bmj.com
Background Intellectual disability (ID) is a neurodevelopmental disorder affecting 1%–3% of
the population worldwide. It is characterised by high phenotypic and genetic heterogeneity …

Homozygous missense mutation in the LMAN2L gene segregates with intellectual disability in a large consanguineous Pakistani family.

R Rafiullah, M Aslamkhan, N Paramasivam… - Journal of Medical …, 2015 - europepmc.org
Background Intellectual disability (ID) is a neurodevelopmental disorder affecting 1%-3% of
the population worldwide. It is characterised by high phenotypic and genetic heterogeneity …

Homozygous missense mutation in the LMAN2L gene segregates with intellectual disability in a large consanguineous Pakistani family

R Rafiullah, M Aslamkhan… - Journal of Medical …, 2016 - search.proquest.com
Background Intellectual disability (ID) is a neurodevelopmental disorder affecting 1%-3% of
the population worldwide. It is characterised by high phenotypic and genetic heterogeneity …

Homozygous missense mutation in the LMAN2L gene segregates with intellectual disability in a large consanguineous Pakistani family

R Rafiullah, M Aslamkhan… - Journal of medical …, 2016 - pubmed.ncbi.nlm.nih.gov
Background Intellectual disability (ID) is a neurodevelopmental disorder affecting 1%-3% of
the population worldwide. It is characterised by high phenotypic and genetic heterogeneity …
[PDF] researchgate.net

[PDF][PDF] Homozygous missense mutation in the LMAN2L gene segregates with intellectual disability in a large consanguineous Pakistani family

R Rafiullah, M Aslamkhan, N Paramasivam, C Thiel… - 2015 - researchgate.net
Background Intellectual disability (ID) is a neurodevelopmental disorder affecting 1%–3% of
the population worldwide. It is characterised by high phenotypic and genetic heterogeneity …
[PDF] uni-augsburg.de

[PDF][PDF] Homozygous missense mutation in the LMAN2L gene segregates with intellectual disability in a large consanguineous Pakistani family

R Rafiullah, M Aslamkhan, N Paramasivam… - 2016 - opus.bibliothek.uni-augsburg.de
Background Intellectual disability (ID) is a neurodevelopmental disorder affecting 1%–3% of
the population worldwide. It is characterised by high phenotypic and genetic heterogeneity …
[PDF] uni-augsburg.de

[PDF][PDF] Homozygous missense mutation in the LMAN2L gene segregates with intellectual disability in a large consanguineous Pakistani family

R Rafiullah, M Aslamkhan, N Paramasivam, C Thiel… - opus.bibliothek.uni-augsburg.de
Background Intellectual disability (ID) is a neurodevelopmental disorder affecting 1%–3% of
the population worldwide. It is characterised by high phenotypic and genetic heterogeneity …