Mutations and polymorphisms in the pyruvate dehydrogenase E1 alpha gene
- PMID: 1301207
- DOI: 10.1002/humu.1380010203
Mutations and polymorphisms in the pyruvate dehydrogenase E1 alpha gene
Abstract
We present an update on mutations and polymorphisms in the human X chromosome located pyruvate dehydrogenase E1 alpha gene. A total of 20 different mutations are tabulated. The mutations include deletions, insertions, and point mutations. Certain sequences seem particularly prone to mutation. Most of the mutations are found in exons 10 and 11. Furthermore, four of the mutations are seen in unrelated patients. Little is known about how the mutations affect the structure or function of the pyruvate dehydrogenase complex.
Similar articles
-
Mutations in the X-linked pyruvate dehydrogenase (E1) alpha subunit gene (PDHA1) in patients with a pyruvate dehydrogenase complex deficiency.Hum Mutat. 2000;15(3):209-19. doi: 10.1002/(SICI)1098-1004(200003)15:3<209::AID-HUMU1>3.0.CO;2-K. Hum Mutat. 2000. PMID: 10679936 Review.
-
Pyruvate dehydrogenase deficiency in a male caused by a point mutation (F205L) in the E1 alpha subunit.Hum Mutat. 1994;3(2):152-5. doi: 10.1002/humu.1380030210. Hum Mutat. 1994. PMID: 8199595 No abstract available.
-
A novel mutation in the dihydrolipoamide dehydrogenase E3 subunit gene (DLD) resulting in an atypical form of alpha-ketoglutarate dehydrogenase deficiency.Hum Mutat. 2005 Mar;25(3):323-4. doi: 10.1002/humu.9319. Hum Mutat. 2005. PMID: 15712224 Review.
-
Analysis of exonic mutations leading to exon skipping in patients with pyruvate dehydrogenase E1 alpha deficiency.Pediatr Res. 2000 Dec;48(6):748-53. doi: 10.1203/00006450-200012000-00008. Pediatr Res. 2000. PMID: 11102541
-
A mutation in the E1 alpha subunit of pyruvate dehydrogenase associated with variable expression of pyruvate dehydrogenase complex deficiency.Pediatr Res. 1992 Aug;32(2):169-74. doi: 10.1203/00006450-199208000-00009. Pediatr Res. 1992. PMID: 1508605
Cited by
-
Mitochondrial Alpha-Keto Acid Dehydrogenase Complexes: Recent Developments on Structure and Function in Health and Disease.Subcell Biochem. 2024;104:295-381. doi: 10.1007/978-3-031-58843-3_13. Subcell Biochem. 2024. PMID: 38963492 Review.
-
Neuropathological findings of a patient with pyruvate dehydrogenase E1 alpha deficiency presenting as a cerebral lactic acidosis.Acta Neuropathol. 1993;85(6):674-8. doi: 10.1007/BF00334680. Acta Neuropathol. 1993. PMID: 8337946
-
Mutations in the X-linked E1 alpha subunit of pyruvate dehydrogenase: exon skipping, insertion of duplicate sequence, and missense mutations leading to the deficiency of the pyruvate dehydrogenase complex.Am J Hum Genet. 1995 Mar;56(3):558-69. Am J Hum Genet. 1995. PMID: 7887409 Free PMC article.
-
MRI features of 4 female patients with pyruvate dehydrogenase E1 alpha deficiency.Pediatr Neurol. 2011 Jul;45(1):57-9. doi: 10.1016/j.pediatrneurol.2011.02.003. Pediatr Neurol. 2011. PMID: 21723463 Free PMC article.
-
Pyruvate dehydrogenase complex deficiency and absence of subunit X.J Inherit Metab Dis. 1998 Feb;21(1):9-16. doi: 10.1023/a:1005351012066. J Inherit Metab Dis. 1998. PMID: 9501264
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases