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A rare case of LORICRIN gene c.684dup mutation associated with Vohwinkel syndrome in a Turkish patient, in silico analysis and literature review

Cuneyd Yavas; Emir Nekay; Asmaa Abuaisha; Yusuf Seflekci; Kubra Turegun; Zafer Turkoglu; Eriscan Melih Kirsoy; Mustafa Dogan
Molecular Biology Reports · Vol. 53, Issue 1 · 2026
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Bibliographic Information

JournalMolecular Biology Reports
PublisherSpringer
Publication Date2026-12-01
Publication Year2026
Volume53
Issue1
Document TypeJournal Article
Print ISSN0301-4851
eISSN1573-4978
DOI10.1007/s11033-025-11257-w

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NARA Access Coverage1973-01-01~Current
Journal Homepagehttps://www.springer.com/journal/11033
Publisher PageOpen Publisher Page
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