A Comprehensive Overview of NF1 Mutations in Iranian Patients-Reference-Cited by-同舟云学术

A Comprehensive Overview of NF1 Mutations in Iranian Patients

Published:2024-07-02 Issue:1 Volume:26 Page:
ISSN:1559-1174
Container-title:NeuroMolecular Medicine
language:en
Short-container-title:Neuromol Med

Author:

Savad Shahram,Modarressi Mohammad-Hossein,Younesi Sarang,Seifi-Alan Mahnaz,Samadaian Niusha,Masoomy Mona,Dianatpour Mehdi,Norouzi Shima,Amidi Saloomeh,Boroumand Amirreza,Ashrafi Mahmoud Reza,Ronagh Alireza,Eslami Maryam,Hashemnejad Maryam,Nourian Shahab,Mohammadi Sanaz,Taheri Amin Mohammad Mahdi,Heidari Morteza,Seifi-Alan Mahin,Shojaaldini Ardakani Hossein,Aghamahdi Fatemeh,Khalilian Sheyda,Ghafouri-Fard Soudeh

Publisher

Springer Science and Business Media LLC

Link

https://link.springer.com/content/pdf/10.1007/s12017-024-08790-5.pdf

Reference86 articles.

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2. Ars, E., Kruyer, H., Morell, M., Pros, E., Serra, E., Ravella, A., Estivill, X., & Lazaro, C. (2003). Recurrent mutations in the NF1 gene are common among neurofibromatosis type 1 patients. Journal of Medical Genetics, 40(6), e82–e82.

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4. Banck, M. S., Kanwar, R., Kulkarni, A. A., Boora, G. K., Metge, F., Kipp, B. R., Zhang, L., Thorland, E. C., Minn, K. T., & Tentu, R. (2013). The genomic landscape of small intestine neuroendocrine tumors. The Journal of Clinical Investigation, 123(6), 2502–2508.

5. Banerjee, S., Dai, Y., Liang, S., Chen, H., Wang, Y., Tang, L., Wu, J., & Huang, H. (2016). A novel mutation in NF1 is associated with diverse intra-familial phenotypic variation and astrocytoma in a Chinese family. Journal of Clinical Neuroscience, 31, 182–184.