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Q42683516
Q42683516
Dataset
https://www.wikidata.org/wiki/Special:EntityData/Q42683516
Q42683516
Dataset
https://www.wikidata.org/wiki/Special:EntityData/Q42683516
about
Exome sequencing identifies a novel frameshift mutation of MYO6 as the cause of autosomal dominant nonsyndromic hearing loss in a Chinese family.
dateModified
2019-06-25T16:27:06Z
http://www.w3.org/2001/XMLSchema#dateTime
version
968,834,353
http://www.w3.org/2001/XMLSchema#integer
identifiers
2
http://www.w3.org/2001/XMLSchema#integer
sitelinks
0
http://www.w3.org/2001/XMLSchema#integer
statements
59
http://www.w3.org/2001/XMLSchema#integer
type
Dataset