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Plectin abnormality in epidermolysis bullosa simplex Ogna: non-responsiveness of basal keratinocytes to some anti-rat plectin antibodies.
Exp Dermatol. 1997 Feb;6(1):41-8. doi: 10.1111/j.1600-0625.1997.tb00144.x.
Exp Dermatol. 1997.
PMID: 9067706
A site-specific plectin mutation causes dominant epidermolysis bullosa simplex Ogna: two identical de novo mutations.
Koss-Harnes D, Høyheim B, Anton-Lamprecht I, Gjesti A, Jørgensen RS, Jahnsen FL, Olaisen B, Wiche G, Gedde-Dahl T Jr.
Koss-Harnes D, et al.
J Invest Dermatol. 2002 Jan;118(1):87-93. doi: 10.1046/j.0022-202x.2001.01591.x.
J Invest Dermatol. 2002.
PMID: 11851880
Free article.
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Life-long course and molecular characterization of the original Dutch family with epidermolysis bullosa simplex with muscular dystrophy due to a homozygous novel plectin point mutation.
Koss-Harnes D, Høyheim B, Jonkman MF, de Groot WP, de Weerdt CJ, Nikolic B, Wiche G, Gedde-Dahl T Jr.
Koss-Harnes D, et al.
Acta Derm Venereol. 2004;84(2):124-31. doi: 10.1080/00015550310007094.
Acta Derm Venereol. 2004.
PMID: 15206692
Free article.
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Pyoderma gangrenosum as a complication of coronary artery bypass grafting.
Koss-Harnes D, Ovrum E, Langeland T.
Koss-Harnes D, et al.
Eur J Cardiothorac Surg. 1995;9(3):163-5. doi: 10.1016/s1010-7940(05)80068-5.
Eur J Cardiothorac Surg. 1995.
PMID: 7786536
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