E-ISSN 1658-8088 | ISSN 1658-807X
 

Case Report

Online Publishing Date:
30 / 06 / 2022

 



How to Cite this Article
Pubmed Style

Blooshi AA, Al-Shamsi A. A novel frameshift homozygous mutation in FAT1 gene causes ptosis, nephropathy, and syndactyly in an Emirati family: case report and literature review. JBCGenetics. 2022; 5(1): 29-34. doi:10.24911/JBCGenetics/183-1645370249


Web Style

Blooshi AA, Al-Shamsi A. A novel frameshift homozygous mutation in FAT1 gene causes ptosis, nephropathy, and syndactyly in an Emirati family: case report and literature review. https://www.jbcgenetics.com/?mno=84531 [Access: March 29, 2024]. doi:10.24911/JBCGenetics/183-1645370249


AMA (American Medical Association) Style

Blooshi AA, Al-Shamsi A. A novel frameshift homozygous mutation in FAT1 gene causes ptosis, nephropathy, and syndactyly in an Emirati family: case report and literature review. JBCGenetics. 2022; 5(1): 29-34. doi:10.24911/JBCGenetics/183-1645370249



Vancouver/ICMJE Style

Blooshi AA, Al-Shamsi A. A novel frameshift homozygous mutation in FAT1 gene causes ptosis, nephropathy, and syndactyly in an Emirati family: case report and literature review. JBCGenetics. (2022), [cited March 29, 2024]; 5(1): 29-34. doi:10.24911/JBCGenetics/183-1645370249



Harvard Style

Blooshi, A. A. & Al-Shamsi, . A. (2022) A novel frameshift homozygous mutation in FAT1 gene causes ptosis, nephropathy, and syndactyly in an Emirati family: case report and literature review. JBCGenetics, 5 (1), 29-34. doi:10.24911/JBCGenetics/183-1645370249



Turabian Style

Blooshi, Abdulla Al, and Aisha Al-Shamsi. 2022. A novel frameshift homozygous mutation in FAT1 gene causes ptosis, nephropathy, and syndactyly in an Emirati family: case report and literature review. Journal of Biochemical and Clinical Genetics, 5 (1), 29-34. doi:10.24911/JBCGenetics/183-1645370249



Chicago Style

Blooshi, Abdulla Al, and Aisha Al-Shamsi. "A novel frameshift homozygous mutation in FAT1 gene causes ptosis, nephropathy, and syndactyly in an Emirati family: case report and literature review." Journal of Biochemical and Clinical Genetics 5 (2022), 29-34. doi:10.24911/JBCGenetics/183-1645370249



MLA (The Modern Language Association) Style

Blooshi, Abdulla Al, and Aisha Al-Shamsi. "A novel frameshift homozygous mutation in FAT1 gene causes ptosis, nephropathy, and syndactyly in an Emirati family: case report and literature review." Journal of Biochemical and Clinical Genetics 5.1 (2022), 29-34. Print. doi:10.24911/JBCGenetics/183-1645370249



APA (American Psychological Association) Style

Blooshi, A. A. & Al-Shamsi, . A. (2022) A novel frameshift homozygous mutation in FAT1 gene causes ptosis, nephropathy, and syndactyly in an Emirati family: case report and literature review. Journal of Biochemical and Clinical Genetics, 5 (1), 29-34. doi:10.24911/JBCGenetics/183-1645370249





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