A report of a pedigree with compound heterozygous mutations in the SLC22A5 gene
IntroductionTo investigate the clinical characteristics and disease outcomes of a pedigree with compound heterozygous mutations in the SLC22A5 gene.MethodsSerum acylcarnitine profiles of patients were analyzed using tandem mass spectrometry. DNA samples isolated from patients and their first-degree...
Shranjeno v:
Main Authors: | Yunguo Zhou (Author), Yucai Liu (Author), Yang Shen (Author), Fang Xu (Author), Fei Xu (Author), Hui Huang (Author), Junkai Duan (Author) |
---|---|
Format: | Knjiga |
Izdano: |
Frontiers Media S.A.,
2023-06-01T00:00:00Z.
|
Teme: | |
Online dostop: | Connect to this object online. |
Oznake: |
Označite
Brez oznak, prvi označite!
|
Podobne knjige/članki
-
A novel compound heterozygous variant of the SLC12A3 gene in Gitelman syndrome pedigree
od: Yixin Chen, et al.
Izdano: (2018) -
Renal hypouricemia caused by novel compound heterozygous mutations in the SLC22A12 gene: a case report with literature review
od: Zhaowei Zhou, et al.
Izdano: (2018) -
Compound heterozygous mutation of SLC25A1 gene in glutaric aciduria type 2
od: Karthikeyan Kadirvel, et al.
Izdano: (2021) -
Novel compound heterozygous pathogenic variants in the SLC3A1 gene in a Chinese family with cystinuria
od: Danhua Liu, et al.
Izdano: (2023) -
A Pedigree Report of a Rare Case of Weill–Marchesani Syndrome with New Compound Heterozygous LTBP2 Mutations
od: Lin Z, et al.
Izdano: (2021)