Items where Author is "Albuloushi, Ahmad"

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Albuloushi, Ahmad, Lovgren, Marie-Louise, Steel, Ainsley, Yeoh, Yeelon, Waters, Alex, 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 login using a UHB Athens Account. Register for Athens here -

This list was generated on Sun Jul 3 05:01:40 2022 UTC.