Abstract
Congenital Hyperinsulinism is a condition with a number of genetic causes, but for the majority of patients, the underlying aetiology is unknown. We present here a rational argument for the use of computational biology as a valuable resource for identifying new candidate genes which may cause disease and for understanding the complex mechanisms which define the pathophysiology of this rare disease. © 2013 Stevens et al; licensee BioMed Central Ltd.
Original language | English |
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Article number | 21 |
Journal | Orphanet Journal of Rare Diseases |
Volume | 8 |
Issue number | 1 |
DOIs | |
Publication status | Published - 2013 |