Inappropriate Gene Activation in FSHD (Q30050619)

https://doi.org/10.1016%2FS0092-8674%2802%2900826-7

25 May 2017

Rossella Tupler

3

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Davide Gabellini

object named as

Davide Gabellini

series ordinal

1

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author name string

Michael R. Green

series ordinal

2

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https://doi.org/10.1016%2FS0092-8674%2802%2900826-7

25 May 2017

language of work or name

English

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publication date

August 2002

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https://doi.org/10.1016%2FS0092-8674%2802%2900826-7

25 May 2017

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https://doi.org/10.1016%2FS0092-8674%2802%2900826-7

25 May 2017

volume

110

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https://doi.org/10.1016%2FS0092-8674%2802%2900826-7

25 May 2017

issue

3

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https://doi.org/10.1016%2FS0092-8674%2802%2900826-7

25 May 2017

page(s)

339-348

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https://doi.org/10.1016%2FS0092-8674%2802%2900826-7

Adenine nucleotide translocase-1, a component of the permeability transition pore, can dominantly induce apoptosis

25 May 2017

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Molecular genetics of facioscapulohumeral muscular dystrophy (FSHD)

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Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3 kb element

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Application of chromosome 4q35-qter marker (pFR-1) for DNA rearrangement of facioscapulohumeral muscular dystrophy patients in Taiwan

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Correlation between fragment size at D4F104S1 and age at onset or at wheelchair use, with a possible generational effect, accounts for much phenotypic variation in 4q35-facioscapulohumeral muscular dystrophy (FSHD)

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Identifiers

DOI

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Fatcat

https://api.fatcat.wiki/v0/release/syzhnfphhndw3btu66lu5wyjeq

30 July 2022

mapped directly with Wikidata item

Fatcat ID

release_syzhnfphhndw3btu66lu5wyjeq

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/syzhnfphhndw3btu66lu5wyjeq

30 July 2022

mapped directly with Wikidata item

OpenCitations bibliographic resource ID

3237839

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

https://api.fatcat.wiki/v0/release/syzhnfphhndw3btu66lu5wyjeq

30 July 2022