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