Research & Innovation
Publications

Founder mutation c.676insC in three unrelated Kindler syndrome families belonging to a particular clan from Pakistan.

#2012

#JOURNAL OF DERMATOLOGY

PMU Authors
Alfred Klausegger, Johann Bauer

All Authors
Pakeeza A Shaiq, Alfred Klausegger, Fawad Muzaffar, Johann Bauer, Muhammad I Khan, Azra Khanum, Raheel Qamar, Ghazala K Raja

Journal association
JOURNAL OF DERMATOLOGY

Abstract

Keywords

DIAGNOSIS, KINDLIN-1

Latest Publication

#2025

#Abstract

Valentin Fischill-Neudeck, Antje van der Zee-Neuen, Margitta B. Beil-Hildebrand Strengthening Professional Health Literacy: A Theory-Based Approach to Empower Nursing Practice

#2025

#Original Article

Margaux Delporte, Johan Verbeeck, Isabella Brambilla, Georg Zimmermann, Geert Molenberghs, Rima Nabbout, Dravet syndrome, REGISTRY; RARE DISEASES; DRAVET SYNDROME; Natural history;

#2025

#Editorial

Eunkyeong Oh, Alberto Lucchini, Peter Nydahl Personalized approaches to ICU Distress

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Paracelsus Medical University (PMU) Research & Innovation Publications

Founder mutation c.676insC in three unrelated...