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Transglutaminase-1 Mutations in Omani Families with Lamellar Ichthyosis

OBJECTIVE: To determine the molecular basis of familial ichthyosis in three Omani families. SUBJECTS AND METHODS: Nine patients from three consanguineous families, A, B, and C, were born with typical features of lamellar ichthyosis subtype including collodion membrane and maintained ectropion, and e...

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書誌詳細
出版年:Med Princ Pract
主要な著者: Al-Naamani, Aisha, Al-Waily, Ahmed, Al-Kindi, Mohammed, Al-Awadi, Maha, Al-Yahyaee, Said Ali
フォーマット: Artigo
言語:Inglês
出版事項: S. Karger AG 2013
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC5586776/
https://ncbi.nlm.nih.gov/pubmed/23689228
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000349914
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