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Dive into the research topics of 'Ichthyosis prematurity syndrome in two Omani siblings, caused by homozygous c.1A > G mutation in the FATP4 gene'. Together they form a unique fingerprint.- Sort by
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Hilal Al Mandhari*, Buthaina Al-Musalhi, Nouh Al Mahroqi, Hilde T. Hilmarsen, Geir J. Braathen, Denis Khnykin
Research output: Contribution to journal › Article › peer-review