7 Article(s)Download |
PMID | Title | Pub. Year | #Total Relationships |
1 | 31654490 | HSD10 mitochondrial disease: p.Leu122Val variant, mild clinical phenotype, and founder effect in French-Canadian patients from Quebec. | 2019 Dec | 1 |
2 | 28875337 | Clinical and molecular analysis of 6 Chinese patients with isoleucine metabolism defects: identification of 3 novel mutations in the HSD17B10 and ACAT1 gene. | 2017 Dec | 2 |
3 | 23834306 | Transcription start sites and epigenetic analysis of the HSD17B10 proximal promoter. | 2013 Jul 8 | 1 |
4 | 19706438 | Mental retardation linked to mutations in the HSD17B10 gene interfering with neurosteroid and isoleucine metabolism. | 2009 Sep 1 | 1 |
5 | 17618155 | HSD17B10: a gene involved in cognitive function through metabolism of isoleucine and neuroactive steroids. | 2007 Sep-Oct | 1 |
6 | 15860413 | Multiple functions of type 10 17beta-hydroxysteroid dehydrogenase. | 2005 May-Jun | 1 |
7 | 11102558 | Progressive infantile neurodegeneration caused by 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency: a novel inborn error of branched-chain fatty acid and isoleucine metabolism. | 2000 Dec | 1 |