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Publications Authored by Mohammed El-Asrag | PubFacts
Mohammed El-Asrag

Mohammed El-Asrag

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11Publications

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LHFPL5 mutation: A rare cause of non-syndromic autosomal recessive hearing loss.

Eur J Med Genet 2018 Nov 23. Epub 2018 Nov 23.

Section of Ophthalmology & Neuroscience, Leeds Institute of Medical Research at St. James's, University of Leeds, United Kingdom. Electronic address:

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Source
https://linkinghub.elsevier.com/retrieve/pii/S17697212183010
Publisher Site
http://dx.doi.org/10.1016/j.ejmg.2018.11.026DOI Listing
November 2018

Homozygous single base deletion in TUSC3 causes intellectual disability with developmental delay in an Omani family.

Am J Med Genet A 2016 07 5;170(7):1826-31. Epub 2016 May 5.

Section of Ophthalmology and Neuroscience, Leeds Institute of Biomedical and Clinical Sciences, University of Leeds, United Kingdom.

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Source
http://dx.doi.org/10.1002/ajmg.a.37690DOI Listing
July 2016