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SDR9C7
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SDR9C7 plays an essential role in skin barrier function by dehydrogenating acylceramide for covalent…
Impaired epidermal barrier in autosomal recessive congenital ichthyosis (ARCI) caused by missense mu…
Identification of mutations in SDR9C7 in six families with autosomal recessive congenital ichthyosis…
Mutations in SDR9C7 gene encoding an enzyme for vitamin A metabolism underlie autosomal recessive co…
Deficient stratum corneum intercellular lipid in a Japanese patient with lamellar ichthyosis with a …
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