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HARVARD Citation
McKenzie, F. et al. (2021). Severe congenital cutis laxa: Identification of novel homozygous LOX gene variants in two families. Clinical genetics. 100 (2), pp. 168-175. [Online].
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McKenzie, F. et al. (2021). Severe congenital cutis laxa: Identification of novel homozygous LOX gene variants in two families. Clinical genetics. 100 (2), pp. 168-175. [Online].