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...

Deskribapen osoa

Xehetasun bibliografikoak
Egile Nagusiak: Juan Luo, Xiaohong Chen, Hongxi Guo, Peiwei Zhao, Hui Yao, Lifang Feng, Luhong Yang
Formatua: Artikulua
Hizkuntza:English
Argitaratua: SpringerOpen 2024-01-01
Saila:Egyptian Journal of Medical Human Genetics
Gaiak:
MTR gene
Hyperhomocysteinemia (HHcy)
Methylcobalamin deficiency G (cblG) disorder
Methionine synthase (MS)
Whole-exome sequencing (WES)
Sarrera elektronikoa:https://doi.org/10.1186/s43042-023-00469-z

Internet

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

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