Albuloushi, A ; Lovgren, M ; Steel, A... Albuloushi , A , Lovgren , M , Steel , A , Yeoh , Y , Waters , A , Zamiri , M & Martin , P E 2020 , ' A heterozygous mutation in GJB2 (Cx26F142L) associated with deafness and recurrent skin rashes results in connexin assembly deficiencies ' , Experimental Dermatology , vol. 29 , no. 10 , pp. 970-979 . https://doi.org/10.1111/exd.14187.
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2020