(Q24320253)

Emery-Dreifuss muscular dystrophy

GOA release 2020-03-11

1 reference

A Nagano

1

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R Koga

2

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M Ogawa

3

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Y Kurano

4

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J Kawada

5

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R Okada

6

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Y K Hayashi

7

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T Tsukahara

8

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K Arahata

https://scigraph.springernature.com/pub.10.1038/ng0396-254

9

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language of work or name

English

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publication date

March 1996

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published in

Nature Genetics

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volume

12

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page(s)

254-9

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issue

3

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exact match

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cites work

Linkage of Emery-Dreifuss muscular dystrophy to the red/green cone pigment (RGCP) genes, proximal to factor VIII.

1 reference

https://api.crossref.org/works/10.1038%2FNG0396-254

Multipoint linkage mapping of the Emery-Dreifuss muscular dystrophy gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0396-254

Dystrophin: the protein product of the Duchenne muscular dystrophy locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0396-254

Immunostaining of skeletal and cardiac muscle surface membrane with antibody against Duchenne muscular dystrophy peptide

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0396-254

A severe muscular dystrophy patient with an internally deleted very short (110 kD) dystrophin: presence of the binding site for dystrophin-associated glycoprotein (DAG) may not be enough for physiological function of dystrophin

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0396-254

Preservation of the C-terminus of dystrophin molecule in the skeletal muscle from Becker muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0396-254

Decreased myotonin-protein kinase in the skeletal and cardiac muscles in myotonic dystrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0396-254

A short history of tissue fractionation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0396-254

Unusual type of benign x-linked muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0396-254

7 January 2021

Emery-Dreifuss muscular dystrophy and other related disorders

1 reference

https://api.crossref.org/works/10.1038%2FNG0396-254

7 January 2021

A linkage study of Emery-Dreifuss muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0396-254

7 January 2021

Localisation of the gene for Emery-Dreifuss muscular dystrophy to the distal long arm of the X chromosome

1 reference

https://api.crossref.org/works/10.1038%2FNG0396-254

7 January 2021

Mapping of the Emery-Dreifuss gene through reconstruction of crossover points in two Italian pedigrees

1 reference

https://api.crossref.org/works/10.1038%2FNG0396-254

7 January 2021

Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0396-254

7 January 2021

Identification of novel mutations in three families with Emery-Dreifuss muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0396-254

7 January 2021

Identification of new mutations in the Emery-Dreifuss muscular dystrophy gene and evidence for genetic heterogeneity of the disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0396-254

7 January 2021

SSCP detection of novel mutations in patients with Emery-Dreifuss muscular dystrophy: definition of a small C-terminal region required for emerin function.

1 reference

https://api.crossref.org/works/10.1038%2FNG0396-254

7 January 2021

Transcriptional organization of a 450-kb region of the human X chromosome in Xq28

1 reference

https://api.crossref.org/works/10.1038%2FNG0396-254

7 January 2021

The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein

1 reference

https://api.crossref.org/works/10.1038%2FNG0396-254

7 January 2021

Dystrophin diagnosis: comparison of dystrophin abnormalities by immunofluorescence and immunoblot analyses

1 reference

https://api.crossref.org/works/10.1038%2FNG0396-254

7 January 2021