Yıl: 2022 Cilt: 28 Sayı: 1 Sayfa Aralığı: 59 - 60 Metin Dili: İngilizce DOI: 10.4274/tnd.2022.77535 İndeks Tarihi: 22-05-2023

Epilepsy and Amelogenesis Imperfecta: Think of Kohlschütter-Tönz Syndrome

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Anahtar Kelime:

Epilepsi ve Amelogenesis İmperfekta: Kohlschütter-Tönz Sendromunu Düşünün

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  • 1. Kohlschütter A, Chappuis D, Meier C, et al. Familial epilepsy and yellow teeth--a disease of the CNS associated with enamel hypoplasia. Helv Paediatr Acta 1974;29:283-294.
  • 2. Schossig A, Wolf NI, Fischer C, et al. Mutations in ROGDI cause Kohlschütter-Tönz syndrome. Am J Hum Genet 2012;90:701-707.
  • 3. Donnai D, Tomlin PI, Winter RM. Kohlschutter syndrome in siblings. Clin Dysmorphol 2005;14:123-126.
  • 4. Schossig A, Bloch-Zupan A, Lussi A, et al. SLC13A5 is the second gene associated with Kohlschütter–Tönz syndrome. J Med Genet 2017;54:54-62.
  • 5. Akgün-Doğan Ö, Simsek-Kiper PO, Taşkıran E, et al. Kohlschütter–Tönz syndrome with a novel ROGD1 variant in 3 individuals: a rare clinical entity. J Child Neurol 2021;36:816-822.
APA SOKMEN O, Dericioglu N (2022). Epilepsy and Amelogenesis Imperfecta: Think of Kohlschütter-Tönz Syndrome. , 59 - 60. 10.4274/tnd.2022.77535
Chicago SOKMEN OKAN,Dericioglu Nese Epilepsy and Amelogenesis Imperfecta: Think of Kohlschütter-Tönz Syndrome. (2022): 59 - 60. 10.4274/tnd.2022.77535
MLA SOKMEN OKAN,Dericioglu Nese Epilepsy and Amelogenesis Imperfecta: Think of Kohlschütter-Tönz Syndrome. , 2022, ss.59 - 60. 10.4274/tnd.2022.77535
AMA SOKMEN O,Dericioglu N Epilepsy and Amelogenesis Imperfecta: Think of Kohlschütter-Tönz Syndrome. . 2022; 59 - 60. 10.4274/tnd.2022.77535
Vancouver SOKMEN O,Dericioglu N Epilepsy and Amelogenesis Imperfecta: Think of Kohlschütter-Tönz Syndrome. . 2022; 59 - 60. 10.4274/tnd.2022.77535
IEEE SOKMEN O,Dericioglu N "Epilepsy and Amelogenesis Imperfecta: Think of Kohlschütter-Tönz Syndrome." , ss.59 - 60, 2022. 10.4274/tnd.2022.77535
ISNAD SOKMEN, OKAN - Dericioglu, Nese. "Epilepsy and Amelogenesis Imperfecta: Think of Kohlschütter-Tönz Syndrome". (2022), 59-60. https://doi.org/10.4274/tnd.2022.77535
APA SOKMEN O, Dericioglu N (2022). Epilepsy and Amelogenesis Imperfecta: Think of Kohlschütter-Tönz Syndrome. Türk Nöroloji Dergisi, 28(1), 59 - 60. 10.4274/tnd.2022.77535
Chicago SOKMEN OKAN,Dericioglu Nese Epilepsy and Amelogenesis Imperfecta: Think of Kohlschütter-Tönz Syndrome. Türk Nöroloji Dergisi 28, no.1 (2022): 59 - 60. 10.4274/tnd.2022.77535
MLA SOKMEN OKAN,Dericioglu Nese Epilepsy and Amelogenesis Imperfecta: Think of Kohlschütter-Tönz Syndrome. Türk Nöroloji Dergisi, vol.28, no.1, 2022, ss.59 - 60. 10.4274/tnd.2022.77535
AMA SOKMEN O,Dericioglu N Epilepsy and Amelogenesis Imperfecta: Think of Kohlschütter-Tönz Syndrome. Türk Nöroloji Dergisi. 2022; 28(1): 59 - 60. 10.4274/tnd.2022.77535
Vancouver SOKMEN O,Dericioglu N Epilepsy and Amelogenesis Imperfecta: Think of Kohlschütter-Tönz Syndrome. Türk Nöroloji Dergisi. 2022; 28(1): 59 - 60. 10.4274/tnd.2022.77535
IEEE SOKMEN O,Dericioglu N "Epilepsy and Amelogenesis Imperfecta: Think of Kohlschütter-Tönz Syndrome." Türk Nöroloji Dergisi, 28, ss.59 - 60, 2022. 10.4274/tnd.2022.77535
ISNAD SOKMEN, OKAN - Dericioglu, Nese. "Epilepsy and Amelogenesis Imperfecta: Think of Kohlschütter-Tönz Syndrome". Türk Nöroloji Dergisi 28/1 (2022), 59-60. https://doi.org/10.4274/tnd.2022.77535