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 Dean Liu + 387 word(s) 387 2020-12-15 07:59:04

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. LAMA2 Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/4358 (accessed on 29 September 2026).
Liu D. LAMA2 Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/4358. Accessed September 29, 2026.
Liu, Dean. "LAMA2 Gene" Encyclopedia, https://encyclopedia.pub/entry/4358 (accessed September 29, 2026).
Liu, D. (2020, December 23). LAMA2 Gene. In Encyclopedia. https://encyclopedia.pub/entry/4358
Liu, Dean. "LAMA2 Gene." Encyclopedia. Web. 23 December, 2020.
LAMA2 Gene
Edit

Laminin subunit alpha 2

genes

References

  1. Allamand V, Guicheney P. Merosin-deficient congenital muscular dystrophy,autosomal recessive (MDC1A, MIM#156225, LAMA2 gene coding for alpha2 chain oflaminin). Eur J Hum Genet. 2002 Feb;10(2):91-4.
  2. Gavassini BF, Carboni N, Nielsen JE, Danielsen ER, Thomsen C, Svenstrup K,Bello L, Maioli MA, Marrosu G, Ticca AF, Mura M, Marrosu MG, Soraru G, AngeliniC, Vissing J, Pegoraro E. Clinical and molecular characterization of limb-girdle muscular dystrophy due to LAMA2 mutations. Muscle Nerve. 2011 Nov;44(5):703-9.doi: 10.1002/mus.22132.
  3. Geranmayeh F, Clement E, Feng LH, Sewry C, Pagan J, Mein R, Abbs S, Brueton L,Childs AM, Jungbluth H, De Goede CG, Lynch B, Lin JP, Chow G, Sousa Cd, O'Mahony O, Majumdar A, Straub V, Bushby K, Muntoni F. Genotype-phenotype correlation in alarge population of muscular dystrophy patients with LAMA2 mutations. NeuromusculDisord. 2010 Apr;20(4):241-50. doi: 10.1016/j.nmd.2010.02.001.
  4. Jones KJ, Morgan G, Johnston H, Tobias V, Ouvrier RA, Wilkinson I, North KN.The expanding phenotype of laminin alpha2 chain (merosin) abnormalities: caseseries and review. J Med Genet. 2001 Oct;38(10):649-57. Review.
  5. Miyagoe-Suzuki Y, Nakagawa M, Takeda S. Merosin and congenital musculardystrophy. Microsc Res Tech. 2000 Feb 1-15;48(3-4):181-91. 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 : Dean Liu
View Times: 711
Entry Collection: MedlinePlus
Revision: 1 time (View History)
Update Date: 23 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