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

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SEEK ID: https://publications.h-its.org/publications/185

SEEK ID: https://publications.h-its.org/publications/185

DOI: 10.1136/jmedgenet-2015-103179

Research Groups: Molecular and Cellular Modeling

Publication type: Journal

Journal: J. Med. Genetics

Citation: J Med Genet 53(2):138-144

Date Published: 21st Jan 2016

Registered Mode: imported from a bibtex file

Authors: Rafiullah Rafiullah, Muhammad Aslamkhan, Nagarajan Paramasivam, Christian Thiel, Ghulam Mustafa, Stefan Wiemann, Matthias Schlesner, Rebecca C Wade, Gudrun A Rappold, Simone Berkel

Citation
Rafiullah, R., Aslamkhan, M., Paramasivam, N., Thiel, C., Mustafa, G., Wiemann, S., Schlesner, M., Wade, R. C., Rappold, G. A., & Berkel, S. (2015). Homozygous missense mutation in theLMAN2Lgene segregates with intellectual disability in a large consanguineous Pakistani family. In Journal of Medical Genetics (Vol. 53, Issue 2, pp. 138–144). BMJ. https://doi.org/10.1136/jmedgenet-2015-103179
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Created: 7th Sep 2019 at 08:19

Last updated: 5th Mar 2024 at 21:23

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