(Q42648925)

4 November 2017

Enrichment of the R77C alpha-sarcoglycan gene mutation in Finnish LGMD2D patients (English)

1 reference

autosomal recessive limb-girdle muscular dystrophy type 2D

4 November 2017

0 references

1 reference

Hackman P

1

1 reference

4 November 2017

Juvonen V

2

1 reference

4 November 2017

Sarparanta J

3

1 reference

4 November 2017

Penttinen M

4

1 reference

4 November 2017

Aärimaa T

5

1 reference

4 November 2017

Uusitalo M

6

1 reference

4 November 2017

Auranen M

7

1 reference

4 November 2017

Pihko H

8

1 reference

4 November 2017

Alén R

9

1 reference

4 November 2017

Junes M

10

1 reference

4 November 2017

Lönnqvist T

11

1 reference

4 November 2017

Kalimo H

12

1 reference

4 November 2017

Udd B

13

1 reference

4 November 2017

1 February 2005

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4 November 2017

1 reference

4 November 2017

31

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4 November 2017

2

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4 November 2017

199-204

1 reference

Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q.

4 November 2017

1 reference

Beta-sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex

21 January 2018

1 reference

Making sense of the limb-girdle muscular dystrophies

21 January 2018

1 reference

Characterization of delta-sarcoglycan, a novel component of the oligomeric sarcoglycan complex involved in limb-girdle muscular dystrophy

21 January 2018

1 reference

Dual origins of Finns revealed by Y chromosome haplotype variation

21 January 2018

1 reference

β–sarcoglycan: characterization and role in limb–girdle muscular dystrophy linked to 4q12

21 January 2018

1 reference

Dystrophin-glycoprotein complex: post-translational processing and dystroglycan function.

21 January 2018

1 reference

Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene

21 January 2018

1 reference

Dystrophin-associated proteins in muscular dystrophy

21 January 2018

1 reference

Linkage analysis in autosomal recessive limb-girdle muscular dystrophy (AR LGMD) maps a sixth form to 5q33-34 (LGMD2F) and indicates that there is at least one more subtype of AR LGMD

21 January 2018

1 reference

Molecular genetics of the Finnish disease heritage.

21 January 2018

1 reference

Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy

21 January 2018

1 reference

Paternal and maternal DNA lineages reveal a bottleneck in the founding of the Finnish population

21 January 2018

1 reference

Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the Brazilian population

21 January 2018

1 reference

The 105th ENMC sponsored workshop: pathogenesis in the non-sarcoglycan limb-girdle muscular dystrophies, Naarden, April 12–14, 2002

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/MUS.20267

1 reference

4 November 2017

1 reference