Orphanet: Diagnostik der famili�ren partiellen Lipodystrophie assoziiert mit PPARG Genmutation

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Diagnosis of familial partial lipodystrophy associated with PPARG mutation

Despite our efforts to ensure that data is up to date, this activity has not been validated since 15/05/2008
  • Molekulargenetisches Labor
  • Zentrum fr Nephrologie und Stoffwechsel
  • Praxis Dr. Mato Nagel
  • Albert-Schweitzer-Ring 32
  • 02943 WEIWASSER
  • Director of laboratory : Ms Sylvi NAGORKA
  • More information
  • Phone : 49 (0)3576 287922
  • Additional Phone : 49 (0)3576 215522
  • Fax : 49 (0)3576 287944/215524
  • Website
  • Contact
Last update: May 2008

Responsible of diagnostic test


Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region
Sanger sequencing

List of diseases and genes

List of diseases tested (1)
List of genes tested (including panels) (1)
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