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JCR 2016
جستجوی مقالات
دوشنبه 24 آذر 1404
Iranian Journal of Blood and Cancer
، جلد ۱۶، شماره ۴، صفحات ۱-۸
عنوان فارسی
چکیده فارسی مقاله
کلیدواژههای فارسی مقاله
عنوان انگلیسی
F8 Gene Splice Donor Mutation (c.1271+1G>A) in Individual with Mild Hemophilia A in Indonesia: A Case Study
چکیده انگلیسی مقاله
Introduction:
Hemophilia A is a bleeding disorder caused by a deficiency of coagulation factor VIII. Hemophilia A is an X-linked recessive disorder. Depending on the level of blood coagulation factor VIII, hemophilia severity is classified as mild (5-40%), moderate (1-5%), or severe (<1%). The absence of hemophilia A mutation studies in Indonesia makes this topic important to study.
Methods:
This study detected and classified
F8
gene mutations. A member of the Indonesian Hemophilia Society Association for the Special Region of Yogyakarta provided saliva for DNA testing. Long-read sequencing data were analyzed using the next-generation sequencing (NGS) technique via the Oxford Nanopore Technologies plc (ONT) PromethION 24 platform. The mutation was confirmed using Sanger sequencing by amplifying intron 8 of the
F8
gene with the PCR technique. The
F8
gene intron 8 nucleotide sequence was aligned using the alignment tool on the Benchling website.
Results:
The results of this study showed that there was a splice donor site mutation in intron 8 of the
F8
gene (c.1271+1G>A) in one patient. This mutation can cause the occurrence of cryptic splice donor sites. Cryptic splice donor site prediction was carried out using the splice donor prediction tool available on the NNSPLICE website. The appearance of cryptic splice donor sites can lead to the formation of out-of-frame proteins.
Conclusions:
The
F8
gene mutation causing hemophilia A was detected using long-read sequencing and the next-generation sequencing (NGS) technique. The type of mutation identified is a splice donor site mutation, specifically the variant c.1271+1G>A, in sample code HM13.
کلیدواژههای انگلیسی مقاله
Hemophilia A, Factor 8 gene, Intron 8, Donor splice mutation, c.1271+1G
نویسندگان مقاله
| Ni Gusti Ayu Galuh Candra Kirana Kirana
Faculty of Biology, Universitas Gadjah Mada, 55281, Yogyakarta, Indonesia
| Suprianto
Faculty of Biology, Universitas Gadjah Mada, 55281, Yogyakarta, Indonesia
| Indra Lesmana Lesmana
Department of Tropical Biology, Faculty of Biology, Universitas Gadjah Mada, 55281, Yogyakarta, Indonesia.
| Usi Sukorini Sukorini
Department of Clinical Pathology and Laboratory Medicine, Universitas Gadjah Mada, 55281, Yogyakarta, Indonesia
| Niken Satuti Nur Handayani Handayani
Department of Tropical Biology, Faculty of Biology, Universitas Gadjah Mada, 55281, Yogyakarta, Indonesia.
نشانی اینترنتی
http://ijbc.ir/browse.php?a_code=A-10-1167-1&slc_lang=en&sid=1
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کد مقاله (doi)
زبان مقاله منتشر شده
en
موضوعات مقاله منتشر شده
Genetics
نوع مقاله منتشر شده
پژوهشی
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