Ichthyosis prematurity syndrome in two Omani siblings, caused by homozygous c.1A > G mutation in the FATP4 gene

Hilal Al Mandhari*, Buthaina Al-Musalhi, Nouh Al Mahroqi, Hilde T. Hilmarsen, Geir J. Braathen, Denis Khnykin

*Corresponding author for this work

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