(Q34405791)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15786463%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

title

Commonality of TRIM32 mutation in causing sarcotubular myopathy and LGMD2H (English)

1 reference

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9 January 2020

1

1 reference

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9 January 2020

Patrick Frosk

2

1 reference

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9 January 2020

Hanns Lochmüller

5

1 reference

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9 January 2020

author name string

Andrew G Engel

3

1 reference

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9 January 2020

Ursula Klutzny

4

1 reference

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9 January 2020

Klaus Wrogemann

6

1 reference

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9 January 2020

publication date

1 April 2005

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9 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15786463%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

volume

57

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9 January 2020

issue

4

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9 January 2020

page(s)

591-595

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A gene for autosomal recessive limb-girdle muscular dystrophy in Manitoba Hutterites maps to chromosome region 9q31-q33: evidence for another limb-girdle muscular dystrophy locus

9 January 2020

cites work

1 reference

Limb-girdle muscular dystrophy type 2H associated with mutation in TRIM32, a putative E3-ubiquitin-ligase gene

21 January 2018

1 reference

The most common mutation in FKRP causing limb girdle muscular dystrophy type 2I (LGMD2I) may have occurred only once and is present in Hutterites and other populations

21 January 2018

1 reference

The tripartite motif family identifies cell compartments

21 January 2018

1 reference

RING protein Trim32 associated with skin carcinogenesis has anti-apoptotic and E3-ubiquitin ligase properties

21 January 2018

1 reference

Cytochemistry of phosphatases of the sarcoplasmic reticulum. II. In situ localization of the Mg-dependent enzyme

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/ANA.20441

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15786463%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

1 reference