Items where Author is "Albuloushi, Ahmad"

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Albuloushi, Ahmad and Lovgren, Marie-Louise and Steel, Ainsley and Yeoh, Yeelon and Waters, Alex and Zamiri, Mozheh and Martin, Patricia E (2020) A heterozygous mutation in GJB2 (Cx26F142L) associated with deafness and recurrent skin rashes results in connexin assembly deficiencies. Experimental dermatology. ISSN 1600-0625. This article is available to all UHB staff and students via ASK Discovery tool http://tinyurl.com/z795c8c by using their UHB Athens login IDs

This list was generated on Thu Oct 22 05:53:13 2020 UTC.