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TOR1AIP1 as a cause of cardiac failure and recessive limb-girdle muscular dystrophy

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Year: 2016
Type: article
Study design: Case Report
Source: Neuromuscular Disorders
DOI: 10.1016/j.nmd.2016.05.013
Authors: Roula Ghaoui, Tatiana Benavides, Monkol Lek, Leigh B. Waddell, Simranpreet Kaur, Kathryn N. North, Daniel G. MacArthur, Nigel F. Clarke, Sandra T. Cooper
Institutions: The University of Sydney, Children's Hospital at Westmead, Westmead Hospital, Broad Institute, Harvard University, Massachusetts General Hospital, Massachusetts Institute of Technology, Royal Children's Hospital, Murdoch Children's Research Institute, Sydney Children's Hospital
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: W2404651638
FWCI: 2.254
Cites: 13
Cited by: 43
Related to: 10
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