(Q47754974)

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13 November 2019

title

Tibial muscular dystrophy--from clinical description to linkage on chromosome 2q31 (English)

1 reference

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13 November 2019

2

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13 November 2019

author name string

B Udd

1

1 reference

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13 November 2019

H Kalimo

3

1 reference

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13 November 2019

J Partanen

4

1 reference

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13 November 2019

L Pulkkinen

5

1 reference

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13 November 2019

A Paetau

6

1 reference

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13 November 2019

L Peltonen

7

1 reference

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13 November 2019

H Somer

8

1 reference

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13 November 2019

publication date

1 June 1998

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13 November 2019

published in

Neuromuscular Disorders

1 reference

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13 November 2019

volume

8

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13 November 2019

issue

5

1 reference

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13 November 2019

page(s)

327-332

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Tibial muscular dystrophy. Late adult-onset distal myopathy in 66 Finnish patients

13 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900024-8

7 January 2021

Muscular dystrophy with separate clinical phenotypes in a large family

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900024-8

7 January 2021

Late onset hereditary distal myopathy

1 reference

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7 January 2021

Nonvacuolar myopathy in a large family with both late adult onset distal myopathy and severe proximal muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900024-8

7 January 2021

Late onset foot-drop muscular dystrophy with rimmed vacuoles

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900024-8

7 January 2021

Limb-girdle type muscular dystrophy in a large family with distal myopathy: homozygous manifestation of a dominant gene?

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900024-8

7 January 2021

Imaging methods reveal unexpected patchy lesions in late onset distal myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900024-8

7 January 2021

Assignment of the tibial muscular dystrophy locus to chromosome 2q31.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900024-8

7 January 2021

Inclusion body myositis and myopathies

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900024-8

7 January 2021

New developments in hereditary inclusion body myopathies

1 reference

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7 January 2021

Titins: giant proteins in charge of muscle ultrastructure and elasticity

1 reference

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7 January 2021

The giant protein titin. Emerging roles in physiology and pathophysiology

1 reference

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7 January 2021

Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900024-8

7 January 2021

Various types of hereditary inclusion body myopathies map to chromosome 9p1-q1

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900024-8

7 January 2021

Gene locus for autosomal recessive distal myopathy with rimmed vacuoles maps to chromosome 9

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900024-8

7 January 2021

Welander hereditary distal myopathy, a molecular genetic comparison to hereditary myopathies with inclusion bodies

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900024-8

7 January 2021

10.1016/S0960-8966(98)00024-8

Identifiers

DOI

1 reference

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13 November 2019

1 reference