Novel MTR compound-heterozygous mutations in a Chinese girl with HHcy due to methionine synthase deficiency, cblG: a case report

Novel MTR compound-heterozygous mutations in a Chinese girl with HHcy due to methionine synthase deficiency, cblG: a case report

Abstract Background The methylcobalamin deficiency G (cblG) disorder, a rare autosomal recessive disease, is attributed to mutations in the MTR gene, resulting in heightened homocysteine levels and reduced methionine and megaloblastic anemia levels. This disease is predominantly diagnosed using MTR...

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Những tác giả chính: Juan Luo, Xiaohong Chen, Hongxi Guo, Peiwei Zhao, Hui Yao, Lifang Feng, Luhong Yang
Định dạng: Bài viết
Ngôn ngữ:English
Được phát hành: SpringerOpen 2024-01-01
Loạt:Egyptian Journal of Medical Human Genetics
Những chủ đề:
MTR gene
Hyperhomocysteinemia (HHcy)
Methylcobalamin deficiency G (cblG) disorder
Methionine synthase (MS)
Whole-exome sequencing (WES)
Truy cập trực tuyến:https://doi.org/10.1186/s43042-023-00469-z

Internet

https://doi.org/10.1186/s43042-023-00469-z

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