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Article

Novel indel mutation of STS underlies a new phenotype of self-healing recessive X-linked ichthyosis.

Journal of dermatological science - 1 Sept 2015

Takeichi Takuya, Sugiura Kazumitsu, Hsu Chao-Kai, Tanahashi Kana, Takama Hiroyuki, Simpson Michael A, McGrath John A, Akiyama Masashi

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Share to DNA Mutational Analysis
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 26169345
DOI: 10.1016/j.jdermsci.2015.07.001

Genes

STS

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

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Novel indel mutation of STS underlies a new phenotype of self-healing recessive X-linked ichthyosis.PMID 26169345Read ↗

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A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients.Semantic proximity Read ↗

Expanding mutation landscape and phenotypic spectrum of autosomal recessive congenital ichthyosis.Semantic proximity Read ↗

Revisiting X-linked congenital ichthyosis.Semantic proximity Read ↗

X-Linked Ichthyosis: New Insights Into a Multi-System DisorderSemantic proximity Read ↗

X-linked recessive ichthyosis in 8 Tunisian patients: awareness of misdiagnosis due to the technical trap of the STS pseudogeneSemantic proximity Read ↗

Extensive postzygotic mosaicism for a novel keratin 10 mutation in epidermolytic ichthyosis.Semantic proximity Read ↗

Genotype-phenotype correlations with TGM1: clustering of mutations in the bathing suit ichthyosis and self-healing collodion baby variants of lamellar ichthyosis.Semantic proximity Read ↗

X-linked and autosomal dominant forms of the ichthyosis in coinheritance.Semantic proximity Read ↗

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