(Q74371555)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11504599%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

title

The significance of type 1 fiber atrophy (hypotrophy) in childhood neuromuscular disorders (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11504599%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

author name string

C Imoto

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11504599%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

I Nonaka

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11504599%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

publication date

1 August 2001

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11504599%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

published in

Brain and Development

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11504599%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

volume

23

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11504599%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11504599%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

page(s)

298-302

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11504599%20AND%20SRC:MED&resulttype=core&format=json

Muscle fiber types: how many and what kind?

10 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900213-3

7 January 2021

Muscle fiber atrophy and degeneration induced by experimental immobility and hindlimb suspension

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900213-3

7 January 2021

A mutation in the human ryanodine receptor gene associated with central core disease

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900213-3

7 January 2021

Mutations in the ryanodine receptor gene in central core disease and malignant hyperthermia

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900213-3

7 January 2021

A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900213-3

7 January 2021

Mutations in the nebulin gene associated with autosomal recessive nemaline myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900213-3

7 January 2021

A gene mutated in X-linked myotubular myopathy defines a new putative tyrosine phosphatase family conserved in yeast

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900213-3

7 January 2021

10.1016/S0387-7604(01)00213-3

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11504599%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

1 reference