Wikidata

(Q51660072)

English

Homozygous MYH7 R1820W mutation results in recessive myosin storage myopathy: scapuloperoneal and respiratory weakness with dilated cardiomyopathy.

scientific article published on 26 January 2015

In more languages

Statements

title
Homozygous MYH7 R1820W mutation results in recessive myosin storage myopathy: scapuloperoneal and respiratory weakness with dilated cardiomyopathy (English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
25666907
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25666907%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 February 2020

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