Your browser does not fully support modern features. Please upgrade for a smoother experience.
Submitted Successfully!
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 Vivi Li + 565 word(s) 565 2020-12-15 07:52:56

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.
Li, V. FGA Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/5519 (accessed on 14 September 2026).
Li V. FGA Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/5519. Accessed September 14, 2026.
Li, Vivi. "FGA Gene" Encyclopedia, https://encyclopedia.pub/entry/5519 (accessed September 14, 2026).
Li, V. (2020, December 25). FGA Gene. In Encyclopedia. https://encyclopedia.pub/entry/5519
Li, Vivi. "FGA Gene." Encyclopedia. Web. 25 December, 2020.
FGA Gene
Edit

Fibrinogen alpha chain

genes

References

  1. Benson MD, Liepnieks J, Uemichi T, Wheeler G, Correa R. Hereditary renalamyloidosis associated with a mutant fibrinogen alpha-chain. Nat Genet. 1993Mar;3(3):252-5.
  2. Neerman-Arbez M, de Moerloose P, Bridel C, Honsberger A, Schönbörner A,Rossier C, Peerlinck K, Claeyssens S, Di Michele D, d'Oiron R, Dreyfus M,Laubriat-Bianchin M, Dieval J, Antonarakis SE, Morris MA. Mutations in thefibrinogen aalpha gene account for the majority of cases of congenitalafibrinogenemia. Blood. 2000 Jul 1;96(1):149-52.
  3. Neerman-Arbez M, de Moerloose P, Honsberger A, Parlier G, Arnuti B, Biron C,Borg JY, Eber S, Meili E, Peter-Salonen K, Ripoll L, Vervel C, d'Oiron R, StaegerP, Antonarakis SE, Morris MA. Molecular analysis of the fibrinogen gene clusterin 16 patients with congenital afibrinogenemia: novel truncating mutations in theFGA and FGG genes. Hum Genet. 2001 Mar;108(3):237-40.
  4. Neerman-Arbez M, Honsberger A, Antonarakis SE, Morris MA. Deletion of thefibrinogen [correction of fibrogen] alpha-chain gene (FGA) causes congenitalafibrogenemia. J Clin Invest. 1999 Jan;103(2):215-8. Erratum in: J Clin Invest1999 Mar;103(5):759.
  5. Neerman-Arbez M. Molecular basis of fibrinogen deficiency. PathophysiolHaemost Thromb. 2006;35(1-2):187-98. Review.
  6. Picken MM, Linke RP. Nephrotic syndrome due to an amyloidogenic mutation infibrinogen A alpha chain. J Am Soc Nephrol. 2009 Aug;20(8):1681-5. doi:10.1681/ASN.2008070813.
  7. Uemichi T, Liepnieks JJ, Benson MD. Hereditary renal amyloidosis with a novel variant fibrinogen. J Clin Invest. 1994 Feb;93(2):731-6.
  8. Weisel JW. Fibrinogen and fibrin. Adv Protein Chem. 2005;70:247-99. Review.
More
Upload a video for this entry
Information
Contributor MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register : Vivi Li
View Times: 1.1K
Entry Collection: MedlinePlus
Revision: 1 time (View History)
Update Date: 25 Dec 2020
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
There is no comment~
${ textCharacter }/${ maxCharacter }
Submit
Cancel
${ selectedItem.replyTextCharacter }/${ selectedItem.replyMaxCharacter }
Submit
Cancel
Confirm
Are you sure to Delete?
Yes No
Academic Video Service