Leucine-sensitive hyperinsulinaemic hypoglycaemia in patients with loss of function mutations in 3-Hydroxyacyl-CoA Dehydrogenase
<p>Abstract</p> <p>Background</p> <p>Loss of function mutations in 3-Hydroxyacyl-CoA Dehydrogenase (<it>HADH</it>) cause protein sensitive hyperinsulinaemic hypoglycaemia (HH). <it>HADH</it> encodes short chain 3-hydroxacyl-CoA dehydrogenase, an...
Main Authors: | , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2012-05-01
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Series: | Orphanet Journal of Rare Diseases |
Subjects: | |
Online Access: | http://www.ojrd.com/content/7/1/25 |