Your browser does not fully support modern features. Please upgrade for a smoother experience.
Submitted Successfully!
+1 credit
Thank you for your contribution! You can also upload a video entry or images related to this topic.
For video creation, please contact our Academic Video Service.
| Version | Summary | Created by | Modification | Content Size | Created at | Operation |
|---|---|---|---|---|---|---|
| 1 | Dean Liu | + 484 word(s) | 484 | 2020-12-15 07:55:47 |
Video Upload Options
We provide professional Academic Video Service to translate complex research into visually appealing presentations. Would you like to try it?
Cite
If you have any further questions, please contact Encyclopedia Editorial Office.
Liu, D. HADH Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/3833 (accessed on 29 September 2026).
Liu D. HADH Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/3833. Accessed September 29, 2026.
Liu, Dean. "HADH Gene" Encyclopedia, https://encyclopedia.pub/entry/3833 (accessed September 29, 2026).
Liu, D. (2020, December 22). HADH Gene. In Encyclopedia. https://encyclopedia.pub/entry/3833
Liu, Dean. "HADH Gene." Encyclopedia. Web. 22 December, 2020.
Copy Citation
Hydroxyacyl-CoA dehydrogenase
genes
References
- Bennett MJ, Russell LK, Tokunaga C, Narayan SB, Tan L, Seegmiller A, BoriackRL, Strauss AW. Reye-like syndrome resulting from novel missense mutations inmitochondrial medium- and short-chain l-3-hydroxy-acyl-CoA dehydrogenase. MolGenet Metab. 2006 Sep-Oct;89(1-2):74-9.
- Clayton PT, Eaton S, Aynsley-Green A, Edginton M, Hussain K, Krywawych S,Datta V, Malingre HE, Berger R, van den Berg IE. Hyperinsulinism in short-chainL-3-hydroxyacyl-CoA dehydrogenase deficiency reveals the importance ofbeta-oxidation in insulin secretion. J Clin Invest. 2001 Aug;108(3):457-65.
- Hussain K, Clayton PT, Krywawych S, Chatziandreou I, Mills P, Ginbey DW,Geboers AJ, Berger R, van den Berg IE, Eaton S. Hyperinsulinism of infancyassociated with a novel splice site mutation in the SCHAD gene. J Pediatr. 2005May;146(5):706-8.
- Kapoor RR, James C, Flanagan SE, Ellard S, Eaton S, Hussain K.3-Hydroxyacyl-coenzyme A dehydrogenase deficiency and hyperinsulinemichypoglycemia: characterization of a novel mutation and severe dietary proteinsensitivity. J Clin Endocrinol Metab. 2009 Jul;94(7):2221-5. doi:10.1210/jc.2009-0423.
- Molven A, Matre GE, Duran M, Wanders RJ, Rishaug U, Njølstad PR, Jellum E,Søvik O. Familial hyperinsulinemic hypoglycemia caused by a defect in the SCHADenzyme of mitochondrial fatty acid oxidation. Diabetes. 2004 Jan;53(1):221-7.
- Yang SY, He XY, Schulz H. 3-Hydroxyacyl-CoA dehydrogenase and short chain3-hydroxyacyl-CoA dehydrogenase in human health and disease. FEBS J. 2005Oct;272(19):4874-83. Review.
More
Information
Subjects:
Genetics & Heredity
Contributor
MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register
:
View Times:
694
Entry Collection:
MedlinePlus
Revision:
1 time
(View History)
Update Date:
22 Dec 2020
Table of Contents
Notice
You are not a member of the advisory board for this topic. If you want to update advisory board member profile, please contact office@encyclopedia.pub.
OK
Confirm
Only members of the Encyclopedia advisory board for this topic are allowed to note entries. Would you like to become an advisory board member of the Encyclopedia?
Yes
No
${ textCharacter }/${ maxCharacter }
Submit
Cancel
Back
Comments
${ item }
|
${ item.createdUser.fullName }
${ item.createdAt }
${ item.vote }
${ item.reply }
Delete
${ reply.createdUser.fullName }
${ reply.createdAt }
${ reply.vote }
Delete
There is no reply to this comment~
${ item.replyTextCharacter }/${ item.replyMaxCharacter }
Submit
Cancel
More
No more~
There is no comment~
${ textCharacter }/${ maxCharacter }
Submit
Cancel
${ selectedItem.replyTextCharacter }/${ selectedItem.replyMaxCharacter }
Submit
Cancel
Confirm
Are you sure to Delete?
Yes
No