(Q82250583)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20012312%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

title

Autosomal dominant nemaline myopathy caused by a novel alpha-tropomyosin 3 mutation (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20012312%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

1 reference

I C Kiphuth

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20012312%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

S Krause

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20012312%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

H B Huttner

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20012312%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

G Dekomien

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20012312%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

T Struffert

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20012312%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

R Schröder

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20012312%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

publication date

10 December 2009

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20012312%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20012312%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

volume

257

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20012312%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20012312%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

page(s)

658-660

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20012312%20AND%20SRC:MED&resulttype=core&format=json

Identification of a founder mutation in TPM3 in nemaline myopathy patients of Turkish origin

15 January 2020

cites work

1 reference

12 December 2020

Mutations of the slow muscle alpha-tropomyosin gene, TPM3, are a rare cause of nemaline myopathy

1 reference

12 December 2020

Mutations and polymorphisms of the skeletal muscle alpha-actin gene (ACTA1).

1 reference

12 December 2020

Mutations in TPM3 are a common cause of congenital fiber type disproportion

1 reference

12 December 2020

Identification of 45 novel mutations in the nebulin gene associated with autosomal recessive nemaline myopathy

1 reference

12 December 2020

TPM3 mutation in one of the original cases of cap disease

1 reference

12 December 2020

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

1 reference

12 December 2020

NEMALINE MYOPATHY. A NEW CONGENITAL MYOPATHY

1 reference

12 December 2020