Work

P1.12 Frequency of genomic deletion mutations in collagen VI myopathies

Year: 2010

Type: article

Source: Neuromuscular Disorders

DOI: 10.1016/j.nmd.2010.07.027

Authors: R.J. Butterfield, K. Swoboda, K.M. Flanigan, C.G. Bonnemann, R.B. Weiss

Institutions: University of Utah, Nationwide Children's Hospital, Children's Hospital of Philadelphia

Language: English

Topic: Muscle Physiology and Disorders

Subfield: Molecular Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W2018538647

FWCI:

Cites:

Cited by:

Related to: 10