Thiamine

solute carrier family 25 member 19 ; Homo sapiens







9 Article(s)
Download
PMID
Title
Pub. Year
#Total Relationships
1 35102031 Clinical and genetic studies of thiamine metabolism dysfunction syndrome-4: case series and review of the literature. 2022 Jul 1 1
2 33544541 SLC25A19 deficiency and bilateral striatal necrosis with polyneuropathy: a new case and review of the literature. 2021 Feb 23 2
3 34587972 Identification and functional analysis of novel SLC25A19 variants causing thiamine metabolism dysfunction syndrome 4. 2021 Sep 29 3
4 31095747 Genetic defects of thiamine transport and metabolism: A review of clinical phenotypes, genetics, and functional studies. 2019 Jul 2
5 31295743 Bilateral Striatal Necrosis with Polyneuropathy with a Novel SLC25A19 (Mitochondrial Thiamine Pyrophosphate Carrier OMIMI*606521) Mutation: Treatable Thiamine Metabolic Disorder-A Report of Two Indian Cases. 2019 Oct 2
6 31506564 Functional analysis of the third identified SLC25A19 mutation causative for the thiamine metabolism dysfunction syndrome 4. 2019 Nov 2
7 27191787 Treatment of genetic defects of thiamine transport and metabolism. 2016 Jul 1
8 24607307 Analysis of thiamine transporter genes in sporadic beriberi. 2014 Apr 2
9 19798730 SLC25A19 mutation as a cause of neuropathy and bilateral striatal necrosis. 2009 Sep 1