Study of deep intronic sequence exonization in a Japanese neonate with a mitochondrial trifunctional protein deficiency (Q47570050)

4 February 2018

title

Study of deep intronic sequence exonization in a Japanese neonate with a mitochondrial trifunctional protein deficiency (English)

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4 February 2018

mitochondrial trifunctional protein deficiency

main subject

maternal health

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author name string

Jamiyan Purevsuren

1

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4 February 2018

Toshiyuki Fukao

2

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4 February 2018

Yuki Hasegawa

3

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4 February 2018

Seiji Fukuda

4

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4 February 2018

Hironori Kobayashi

5

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4 February 2018

Seiji Yamaguchi

6

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4 February 2018

publication date

9 August 2008

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4 February 2018

Molecular Genetics and Metabolism

published in

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4 February 2018

volume

95

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4 February 2018

issue

1-2

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4 February 2018

page(s)

46-51

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4 February 2018

Structural analysis of cDNAs for subunits of human mitochondrial fatty acid beta-oxidation trifunctional protein

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inferred from DOI database lookup

7 January 2021

based on heuristic

Molecular basis of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of two new mutations

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inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/J.YMGME.2008.06.013

1 reference

4 February 2018

1 reference

4 February 2018