Have a personal or library account? Click to login
Case Report for Two Siblings Carrying Neurofibromatosis Type 1 with a Rare NF1: c.5392C>T Mutation Cover

Case Report for Two Siblings Carrying Neurofibromatosis Type 1 with a Rare NF1: c.5392C>T Mutation

Balkan Journal of Medical Genetics
Volume 24 (2021): Issue 2 (November 2021)
By: DB Sayın Kocakap,  Ö Gündüz,  L Özer and  M Durak  
Open Access
|Jun 2022

Authors

DB Sayın Kocakap

dsayin@yahoo.com

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
Journal RSS Feed
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
Keywords:
Familial,
Mutation,
Neurofibromatosis type 1 (NF1)
Related subjects:
Medicine,
Basic medical science,
Basic medical science, other

© 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.

Previous articleVolume 24 (2021): Issue 2 (November 2021)Next article