Literature DB >> 1301207

Mutations and polymorphisms in the pyruvate dehydrogenase E1 alpha gene.

H H Dahl1, G K Brown, R M Brown, L L Hansen, D S Kerr, I D Wexler, M S Patel, L De Meirleir, W Lissens, K Chun.   

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.

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Year:  1992        PMID: 1301207     DOI: 10.1002/humu.1380010203

Source DB:  PubMed          Journal:  Hum Mutat        ISSN: 1059-7794            Impact factor:   4.878


  23 in total

1.  A case of PDH-E1 alpha mosaicism in a male patient with severe metabolic lactic acidosis.

Authors:  A Seyda; K Chun; S Packman; B H Robinson
Journal:  J Inherit Metab Dis       Date:  2001-10       Impact factor: 4.982

2.  Pyruvate dehydrogenase-e1α deficiency presenting as recurrent demyelination: an unusual presentation and a novel mutation.

Authors:  Pratibha Singhi; Linda De Meirleir; Willy Lissens; Sunit Singhi; Arushi Gahlot Saini
Journal:  JIMD Rep       Date:  2013-02-12

Review 3.  Disorders of pyruvate carboxylase and the pyruvate dehydrogenase complex.

Authors:  B H Robinson; N MacKay; K Chun; M Ling
Journal:  J Inherit Metab Dis       Date:  1996       Impact factor: 4.982

4.  MRI features of 4 female patients with pyruvate dehydrogenase E1 alpha deficiency.

Authors:  Nicholas Ah Mew; Johanna B Loewenstein; Nadja Kadom; Uta Lichter-Konecki; Andrea L Gropman; Jodie M Martin; Adeline Vanderver
Journal:  Pediatr Neurol       Date:  2011-07       Impact factor: 3.372

5.  The SR protein SC35 is responsible for aberrant splicing of the E1alpha pyruvate dehydrogenase mRNA in a case of mental retardation with lactic acidosis.

Authors:  Mathieu Gabut; Manuèle Miné; Cécile Marsac; Michèle Brivet; Jamal Tazi; Johann Soret
Journal:  Mol Cell Biol       Date:  2005-04       Impact factor: 4.272

Review 6.  Pyruvate dehydrogenase deficiency.

Authors:  G K Brown; L J Otero; M LeGris; R M Brown
Journal:  J Med Genet       Date:  1994-11       Impact factor: 6.318

Review 7.  Pyruvate dehydrogenase E1 alpha deficiency: males and females differ yet again.

Authors:  H H Dahl
Journal:  Am J Hum Genet       Date:  1995-03       Impact factor: 11.025

8.  Characterization of a point mutation in the pyruvate dehydrogenase E1 alpha gene from two boys with primary lactic acidaemia.

Authors:  H Awata; F Endo; A Tanoue; A Kitano; I Matsuda
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982

9.  A novel Y243S mutation in the pyruvate dehydrogenase El alpha gene subunit: correlation with thiamine pyrophosphate interaction.

Authors:  C Benelli; F Fouque; I Redonnet-Vernhet; M Malgat; D Fontan; C Marsac; R Dey
Journal:  J Inherit Metab Dis       Date:  2002-08       Impact factor: 4.982

10.  Neuropathological findings of a patient with pyruvate dehydrogenase E1 alpha deficiency presenting as a cerebral lactic acidosis.

Authors:  A Michotte; L De Meirleir; W Lissens; R Denis; J L Wayenberg; I Liebaers; J M Brucher
Journal:  Acta Neuropathol       Date:  1993       Impact factor: 17.088

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