Associated Papers
Infantile Cataracts Associated with a Homozygous Missense MSMO1 Variant-Case Report and Literature Review.
Hassas N et al.
Reports (mdpi), 2026
New Homozygous Missense MSMO1 Mutation in Two Siblings with SC4MOL Deficiency Presenting with Psoriasiform Dermatitis.
Kalay Yildizhan I et al.
Cytogenetic and Genome Research, 2020
The role of sterol-C4-methyl oxidase in epidermal biology.
He M et al.
Biochimica Et Biophysica Acta, 2014
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