LAMC2 Gene

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Liu, D. LAMC2 Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/4368 (accessed on 29 September 2026).

Liu D. LAMC2 Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/4368. Accessed September 29, 2026.

Liu, Dean. "LAMC2 Gene" Encyclopedia, https://encyclopedia.pub/entry/4368 (accessed September 29, 2026).

Liu, D. (2020, December 23). LAMC2 Gene. In Encyclopedia. https://encyclopedia.pub/entry/4368

Liu, Dean. "LAMC2 Gene." Encyclopedia. Web. 23 December, 2020.

LAMC2 Gene

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This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/gene/lamc2

Laminin subunit gamma 2

genes

References

Aumailley M, Bruckner-Tuderman L, Carter WG, Deutzmann R, Edgar D, Ekblom P,Engel J, Engvall E, Hohenester E, Jones JC, Kleinman HK, Marinkovich MP, MartinGR, Mayer U, Meneguzzi G, Miner JH, Miyazaki K, Patarroyo M, Paulsson M, QuarantaV, Sanes JR, Sasaki T, Sekiguchi K, Sorokin LM, Talts JF, Tryggvason K, Uitto J, Virtanen I, von der Mark K, Wewer UM, Yamada Y, Yurchenco PD. A simplifiedlaminin nomenclature. Matrix Biol. 2005 Aug;24(5):326-32. Review.
Castiglia D, Posteraro P, Spirito F, Pinola M, Angelo C, Puddu P, Meneguzzi G,Zambruno G. Novel mutations in the LAMC2 gene in non-Herlitz junctionalepidermolysis bullosa: effects on laminin-5 assembly, secretion, and deposition. J Invest Dermatol. 2001 Sep;117(3):731-9.
Hartwig B, Borm B, Schneider H, Arin MJ, Kirfel G, Herzog V.Laminin-5-deficient human keratinocytes: defective adhesion results in asaltatory and inefficient mode of migration. Exp Cell Res. 2007 May1;313(8):1575-87.
Mühle C, Jiang QJ, Charlesworth A, Bruckner-Tuderman L, Meneguzzi G, SchneiderH. Novel and recurrent mutations in the laminin-5 genes causing lethal junctionalepidermolysis bullosa: molecular basis and clinical course of Herlitz disease.Hum Genet. 2005 Jan;116(1-2):33-42.
Nakano A, Chao SC, Pulkkinen L, Murrell D, Bruckner-Tuderman L, Pfendner E,Uitto J. Laminin 5 mutations in junctional epidermolysis bullosa: molecular basisof Herlitz vs. non-Herlitz phenotypes. Hum Genet. 2002 Jan;110(1):41-51.
Pulkkinen L, Uitto J. Mutation analysis and molecular genetics ofepidermolysis bullosa. Matrix Biol. 1999 Feb;18(1):29-42. Review.
Schneider H, Mühle C, Pacho F. Biological function of laminin-5 and pathogenicimpact of its deficiency. Eur J Cell Biol. 2007 Dec;86(11-12):701-17.
Varki R, Sadowski S, Pfendner E, Uitto J. Epidermolysis bullosa. I. Molecular genetics of the junctional and hemidesmosomal variants. J Med Genet. 2006Aug;43(8):641-52.

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Subjects: Genetics & Heredity

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Update Date: 23 Dec 2020

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