Orphanet: Molekulare Diagnostik der Lipodystrophie BSCL2, LMNA, PPARG und ZMPSTE24 Gen
x

Search for a diagnostic test

* (*) mandatory field

Molecular diagnosis of Lipodystrophy (BSCL2, LMNA, PPARG, and ZMPSTE24 genes)

  • Phone : +43 (0)1 9580164
  • Additional Phone : -
  • Fax : +43 (0)1 8907943
  • Website
  • Contact
Last update: November 2017

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region
Sanger sequencing
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.