Commonality of TRIM32 mutation in causing sarcotubular myopathy and LGMD2H. (Q34405791)

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9 January 2020

title

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

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9 January 2020

1

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Patrick Frosk

2

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9 January 2020

Hanns Lochmüller

5

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9 January 2020

author name string

Andrew G Engel

3

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Ursula Klutzny

4

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Klaus Wrogemann

6

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publication date

1 April 2005

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9 January 2020

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volume

57

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issue

4

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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

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

21 January 2018

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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

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

21 January 2018

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

21 January 2018

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21 January 2018

Identifiers

DOI

10.1002/ANA.20441

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9 January 2020

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