Insights and future directions of potential genetic therapy for Apert syndrome: A systematic review

Author:

Al-Namnam Nisreen MohammedORCID,Jayash Soher NagiORCID,Hariri FirdausORCID,Rahman Zainal Ariff Abdul,Alshawsh Mohammed AbdullahORCID

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,Molecular Medicine

Reference48 articles.

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2. Panigrahi I. Craniosynostosis genetics: the mystery unfolds. Indian J Hum Genet. 2011;17:48.

3. Liu C, Cui Y, Luan J, Zhou X, Han J. The molecular and cellular basis of Apert syndrome. Intractable Rare Diseases Res. 2013;2:115.

4. Kreiborg S, Cohen M Jr. The oral manifestations of Apert syndrome. J Craniofacial Genet Dev Biol. 1991;12:41–8.

5. ŞOANCĂ A, Dudea D, Gocan H, Roman A, Culic B. Oral manifestations in Apert syndrome: case presentation and a brief review of the literature. Romanian J Morphol Embryol. 2010;51:581–4.

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