| Case Report Online Published: 04 Jan 2021 | ||
JBCGenetics. 2021; 4(1): 56-63 | ||
| How to Cite this Article |
| Pubmed Style Alshamsi AM, Shaukat QR, Alkuwaiti MH. Congenital myasthenic syndrome type 23 caused by a missense homozygous c.205G>T (p.Asp69Tyr) in SLC25A1 gene in four Emirati patients from a single family. JBCGenetics. 2021; 4(1): 56-63. doi:10.24911/JBCGenetics/183-1602852756 Web Style Alshamsi AM, Shaukat QR, Alkuwaiti MH. Congenital myasthenic syndrome type 23 caused by a missense homozygous c.205G>T (p.Asp69Tyr) in SLC25A1 gene in four Emirati patients from a single family. https://www.jbcgenetics.com/?mno=14807 [Access: March 12, 2025]. doi:10.24911/JBCGenetics/183-1602852756 AMA (American Medical Association) Style Alshamsi AM, Shaukat QR, Alkuwaiti MH. Congenital myasthenic syndrome type 23 caused by a missense homozygous c.205G>T (p.Asp69Tyr) in SLC25A1 gene in four Emirati patients from a single family. JBCGenetics. 2021; 4(1): 56-63. doi:10.24911/JBCGenetics/183-1602852756 Vancouver/ICMJE Style Alshamsi AM, Shaukat QR, Alkuwaiti MH. Congenital myasthenic syndrome type 23 caused by a missense homozygous c.205G>T (p.Asp69Tyr) in SLC25A1 gene in four Emirati patients from a single family. JBCGenetics. (2021), [cited March 12, 2025]; 4(1): 56-63. doi:10.24911/JBCGenetics/183-1602852756 Harvard Style Alshamsi, A. M., Shaukat, . Q. R. & Alkuwaiti, . M. H. (2021) Congenital myasthenic syndrome type 23 caused by a missense homozygous c.205G>T (p.Asp69Tyr) in SLC25A1 gene in four Emirati patients from a single family. JBCGenetics, 4 (1), 56-63. doi:10.24911/JBCGenetics/183-1602852756 Turabian Style Alshamsi, Aisha M., Qudsia R. Shaukat, and Mohammed H. Alkuwaiti. 2021. Congenital myasthenic syndrome type 23 caused by a missense homozygous c.205G>T (p.Asp69Tyr) in SLC25A1 gene in four Emirati patients from a single family. Journal of Biochemical and Clinical Genetics, 4 (1), 56-63. doi:10.24911/JBCGenetics/183-1602852756 Chicago Style Alshamsi, Aisha M., Qudsia R. Shaukat, and Mohammed H. Alkuwaiti. "Congenital myasthenic syndrome type 23 caused by a missense homozygous c.205G>T (p.Asp69Tyr) in SLC25A1 gene in four Emirati patients from a single family." Journal of Biochemical and Clinical Genetics 4 (2021), 56-63. doi:10.24911/JBCGenetics/183-1602852756 MLA (The Modern Language Association) Style Alshamsi, Aisha M., Qudsia R. Shaukat, and Mohammed H. Alkuwaiti. "Congenital myasthenic syndrome type 23 caused by a missense homozygous c.205G>T (p.Asp69Tyr) in SLC25A1 gene in four Emirati patients from a single family." Journal of Biochemical and Clinical Genetics 4.1 (2021), 56-63. Print. doi:10.24911/JBCGenetics/183-1602852756 APA (American Psychological Association) Style Alshamsi, A. M., Shaukat, . Q. R. & Alkuwaiti, . M. H. (2021) Congenital myasthenic syndrome type 23 caused by a missense homozygous c.205G>T (p.Asp69Tyr) in SLC25A1 gene in four Emirati patients from a single family. Journal of Biochemical and Clinical Genetics, 4 (1), 56-63. doi:10.24911/JBCGenetics/183-1602852756 |
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