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Expanding the clinical phenotype associated with NIPAL4 mutation: Study of a Tunisian consanguineous family with erythrokeratodermia variabilis—Like Autosomal Recessive Congenital Ichthyosis
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Cherine Charfeddine ,
Roles Conceptualization, Data curation, Investigation, Methodology, Visualization, Writing – original draft
* E-mail: cherine.charfeddine@gmail.com
Affiliations University Tunis El Manar, Institut Pasteur de Tunis, Biomedical Genomics and Oncogenetics Laboratory, LR20IPT05, Tunis, Tunisia, Université de la Manouba, Institut de Biotechnologie de Sidi Thabet, Ariana, Tunisia
⨯ - Nadia Laroussi,
- Rahma Mkaouar,
- Raja Jouini,
- Olfa Khayat,
- Aladin Redissi,
- Amor Mosbah,
- Hamza Dallali,
- Achraf Chedly Debbiche,
- Anissa Zaouak,
- Sami Fenniche,
- Sonia Abdelhak,
- Houda Hammami-Ghorbel
https://orcid.org/0000-0002-4656-2661
Expanding the clinical phenotype associated with NIPAL4 mutation: Study of a Tunisian consanguineous family with erythrokeratodermia variabilis—Like Autosomal Recessive Congenital Ichthyosis
- Cherine Charfeddine,
- Nadia Laroussi,
- Rahma Mkaouar,
- Raja Jouini,
- Olfa Khayat,
- Aladin Redissi,
- Amor Mosbah,
- Hamza Dallali,
- Achraf Chedly Debbiche,
- Anissa Zaouak
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- Published: October 20, 2021
- https://doi.org/10.1371/journal.pone.0258777