Friedreich's ataxia protein: phylogenetic evidence for mitochondrial dysfunction (Q56918650)

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21 October 2019

title

Friedreich's ataxia protein: phylogenetic evidence for mitochondrial dysfunction (English)

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21 October 2019

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3

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21 October 2019

Peer Bork

series ordinal

5

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21 October 2019

2

Koonin EV

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21 October 2019

author name string

Gibson TJ

series ordinal

1

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21 October 2019

Pastore A

series ordinal

4

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21 October 2019

publication date

1 November 1996

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21 October 2019

number of pages

4

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inferred from page(s)

published in

Trends in Neurosciences

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21 October 2019

volume

19

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issue

11

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21 October 2019

page(s)

465-468

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Mitochondrial myopathies: genetic defects

21 October 2019

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Early-onset ataxia with cardiomyopathy and retained tendon reflexes maps to the friedreich's ataxia locus on chromosome 9q

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Late onset Friedreich's disease: clinical features and mapping of mutation to the FRDA locus

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Ataxia with isolated vitamin E deficiency is caused by mutations in the alpha-tocopherol transfer protein

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Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion

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Applying motif and profile searches

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The Minimal Gene Complement of Mycoplasma genitalium

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Identifiers

DOI

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21 October 2019

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