Case Report for Two Siblings Carrying Neurofibromatosis Type 1 with a Rare NF1: c.5392C>T Mutation
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Authors
DB Sayın Kocakap
Department of Medical Genetics, Kırıkkale University Faculty of Medicine, Kırıkkale, Turkey
Ö Gündüz
Department of Dermatology, Kırıkkale University Faculty of Medicine, Kırıkkale, Turkey
L Özer
Mikrogen Genetic Diagnostic Laboratory, Ankara, Turkey
M Durak
Department of Dermatology, Kırıkkale University Faculty of Medicine, Kırıkkale, Turkey
DOI: https://doi.org/10.2478/bjmg-2021-0021 | Journal eISSN: 2199-5761
Language: English
Page range: 99 - 102
Published on: Jun 5, 2022
Published by: Macedonian Academy of Sciences and Arts
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year
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© 2022 DB Sayın Kocakap, Ö Gündüz, L Özer, M Durak, published by Macedonian Academy of Sciences and Arts
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.