Paracelsus Medizinische Privatuniversität (PMU)

Forschung & Innovation
Publikationen

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

#2012
#JOURNAL OF DERMATOLOGY

PMU Autor*innen
Alfred Klausegger, Johann Bauer

Alle Autor*innen
Pakeeza A Shaiq, Alfred Klausegger, Fawad Muzaffar, Johann Bauer, Muhammad I Khan, Azra Khanum, Raheel Qamar, Ghazala K Raja

Fachzeitschrift
JOURNAL OF DERMATOLOGY

Kurzfassung

Keywords

DIAGNOSIS, KINDLIN-1