Work

Using whole exome sequencing to identify the mutation causing oculopharyngodistal myopathy

Year: 2012

Type: conference-paper

Source: Newcastle University ePrints (Newcastle Univesity)

DOI: 10.25405/ncl.34184829

Authors: M. Wagner, S. Laval, J. Mueller, H. Durmus, P. Serdaroglu-Oflazer, H. Lochmueller

Language: English

Topic: Genomics and Rare Diseases

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: green

OpenAlex ID: W7220934858

FWCI:

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