Associated Papers
Compound heterozygous ABCA12 variants identified in a Chinese patient with congenital ichthyosiform erythroderma: Advancing genotype-phenotype correlations and literature review.
Liu JW et al.
Molecular Genetics & Genomic Medicine, 2024
38702946 (PubMed )
Supplement: MGG3-12-e2431-s001.docx
Case of harlequin ichthyosis in preterm infant with a compound heterozygous ABCA12 missense mutation.
Miyazaki M et al.
The Journal of Dermatology, 2022
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