The genes for nicein/kalinin 125- and 100-kDa subun... [Genomics. 1994] - PubMed

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Herlitz's junctional epidermolysis bullosa is linked to mutations in the gene (LAMC2) for the gamma 2 subunit of nicein/kalinin (LAMININ-5). [Nat Genet. 1994]
Herlitz's junctional epidermolysis bullosa is linked to mutations in the gene (LAMC2) for the gamma 2 subunit of nicein/kalinin (LAMININ-5).
Aberdam D, Galliano MF, Vailly J, Pulkkinen L, Bonifas J, Christiano AM, Tryggvason K, Uitto J, Epstein EH Jr, Ortonne JP. Nat Genet. 1994 Mar; 6(3):299-304.
Mutations in the gamma 2 chain gene (LAMC2) of kalinin/laminin 5 in the junctional forms of epidermolysis bullosa. [Nat Genet. 1994]
Mutations in the gamma 2 chain gene (LAMC2) of kalinin/laminin 5 in the junctional forms of epidermolysis bullosa.
Pulkkinen L, Christiano AM, Airenne T, Haakana H, Tryggvason K, Uitto J. Nat Genet. 1994 Mar; 6(3):293-7.
Maternal uniparental meroisodisomy in the LAMB3 region of chromosome 1 results in lethal junctional epidermolysis bullosa. [J Invest Dermatol. 1998]
Maternal uniparental meroisodisomy in the LAMB3 region of chromosome 1 results in lethal junctional epidermolysis bullosa.
Takizawa Y, Pulkkinen L, Shimizu H, Lin L, Hagiwara S, Nishikawa T, Uitto J. J Invest Dermatol. 1998 May; 110(5):828-31.
Review The alpha-3 polypeptide chain of laminin 5: insight into wound healing responses from the study of genodermatoses. [Clin Exp Dermatol. 2005]
Review The alpha-3 polypeptide chain of laminin 5: insight into wound healing responses from the study of genodermatoses.
Hamill KJ, McLean WH. Clin Exp Dermatol. 2005 Jul; 30(4):398-404.
Review [Bart syndrome associated to lethal junctional epidermolysis bullosa (Herlitz form)]. [Actas Dermosifiliogr. 2006]
Review [Bart syndrome associated to lethal junctional epidermolysis bullosa (Herlitz form)].
Casanova JM, Martí RM, Baradad M, Egido R, Mascaró JM. Actas Dermosifiliogr. 2006 Dec; 97(10):658-61.

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Cited by 4 PubMed Central articles

A preliminary gene map for the Van der Woude syndrome critical region derived from 900 kb of genomic sequence at 1q32-q41. [Genome Res. 2000]
A preliminary gene map for the Van der Woude syndrome critical region derived from 900 kb of genomic sequence at 1q32-q41.
Schutte BC, Bjork BC, Coppage KB, Malik MI, Gregory SG, Scott DJ, Brentzell LM, Watanabe Y, Dixon MJ, Murray JC. Genome Res. 2000 Jan; 10(1):81-94.
Maternal uniparental disomy of chromosome 1 with reduction to homozygosity of the LAMB3 locus in a patient with Herlitz junctional epidermolysis bullosa. [Am J Hum Genet. 1997]
Maternal uniparental disomy of chromosome 1 with reduction to homozygosity of the LAMB3 locus in a patient with Herlitz junctional epidermolysis bullosa.
Pulkkinen L, Bullrich F, Czarnecki P, Weiss L, Uitto J. Am J Hum Genet. 1997 Sep; 61(3):611-9.
Detection of novel LAMC2 mutations in Herlitz junctional epidermolysis Bullosa. [Mol Med. 1997]
Detection of novel LAMC2 mutations in Herlitz junctional epidermolysis Bullosa.
Pulkkinen L, McGrath J, Airenne T, Haakana H, Tryggvason K, Kivirikko S, Meneguzzi G, Ortonne JP, Christiano AM, Uitto J. Mol Med. 1997 Feb; 3(2):124-35.

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The genes for nicein/kalinin 125- and 100-kDa subunits, candidates for junctiona...
The genes for nicein/kalinin 125- and 100-kDa subunits, candidates for junctional epidermolysis bullosa, map to chromosomes 1q32 and 1q25-q31.
Genomics. 1994 May 1 ;21(1):286-8.

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The genes for nicein/kalinin 125- and 100-kDa subunits, candidates for junctional epidermolysis bullosa, map to chromosomes 1q32 and 1q25-q31.

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