Forschung & Innovation
Publikationen

Novel KIND1 gene mutation in Kindler syndrome with severe gastrointestinal tract involvement.

#2006

#ARCHIVES OF DERMATOLOGY

PMU Autor*innen
Alfred Klausegger, Wolfgang Muss, Martin Laimer, Johann Bauer, Helmut Hintner

Alle Autor*innen
Elke Sadler, Alfred Klausegger, Wolfgang Muss, Ursula Deinsberger, Gabriele Pohla-Gubo, Martin Laimer, Christoph Lanschuetzer, Johann Bauer, Helmut Hintner

Fachzeitschrift
ARCHIVES OF DERMATOLOGY

Kurzfassung

Keywords

PROTEIN, PATHOLOGY, DISORDER, EPIDERMOLYSIS-BULLOSA, ULTRASTRUCTURAL FINDINGS, KINDLIN-1

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Paracelsus Medizinische Privatuniversität Forschung & Innovation Publikationen

Novel KIND1 gene mutation in Kindler syndrome with...