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A Tunisian family with a novel mutation in the gene CYP4F22 for lamellar ichthyosis and co-occurrence of hearing loss in a child due to mutation in the SLC26A4 gene.
Int J Dermatol
; 58(12): 1439-1443, 2019 Dec.
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en Inglés
| MEDLINE | ID: mdl-31020658
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