Novel Missense Mutation A789V in IQSEC2 Underlies X-Linked Intellectual Disability in the MRX78 Family

V M Kalscheuer; V M James; M L Himelright; P Long; Renske Oegema; C Jensen; M Bienek; H Hu; S A Haas; M Topf; Jeannette Hoogeboom; K Harvey; R Walikonis; RJ Harvey

doi:10.3389/fnmol.2015.00085

Novel Missense Mutation A789V in IQSEC2 Underlies X-Linked Intellectual Disability in the MRX78 Family

V M Kalscheuer, V M James, M L Himelright, P Long, Renske Oegema, C Jensen, M Bienek, H Hu, S A Haas, M Topf, Jeannette Hoogeboom, K Harvey, R Walikonis, RJ Harvey

Clinical Genetics

Research output: Contribution to journal › Article › Academic › peer-review

23 Citations (Scopus)

Original language	Undefined/Unknown
Article number	85
Journal	Frontiers in Molecular Neuroscience
Volume	8
DOIs	https://doi.org/10.3389/fnmol.2015.00085
Publication status	Published - 2016

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10.3389/fnmol.2015.00085

http://hdl.handle.net/1765/91669

Cite this

Kalscheuer, V. M., James, V. M., Himelright, M. L., Long, P., Oegema, R., Jensen, C., Bienek, M., Hu, H., Haas, S. A., Topf, M., Hoogeboom, J., Harvey, K., Walikonis, R., & Harvey, RJ. (2016). Novel Missense Mutation A789V in IQSEC2 Underlies X-Linked Intellectual Disability in the MRX78 Family. Frontiers in Molecular Neuroscience, 8, [85]. https://doi.org/10.3389/fnmol.2015.00085

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AU - Kalscheuer, V M

AU - James, V M

AU - Himelright, M L

AU - Long, P

AU - Oegema, Renske

AU - Jensen, C

AU - Bienek, M

AU - Hu, H

AU - Haas, S A

AU - Topf, M

AU - Hoogeboom, Jeannette

AU - Harvey, K

AU - Walikonis, R

AU - Harvey, RJ

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JO - Frontiers in Molecular Neuroscience

JF - Frontiers in Molecular Neuroscience

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