Search for a diagnostic test

* (*) mandatory field

Diagnosis of limb-girdle muscular dystrophy type 2A-N, 2O, 2Q(ANO5, CAPN3, DYSF, FKRP, FKTN, PLEC, POMGNT1, POMT1, POMT2, SGCA, SGCB, SGCD, SGCG, TCAP, TRIM32 and TTN)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 13/01/2015
  • MVZ Dr. Eberhard und Partner - Bereich Laboratoriumsmedizin und Humangenetik
  • Medizinisches Versorgungszentrum (MVZ) Dr. Eberhard und Partner
  • Brauhausstrae 4
  • 44137 DORTMUND
  • Director of laboratory : -
  • More information
  • Phone : 49 (0)231 95720
  • Additional Phone : -
  • Fax : 49 (0)231 553619
  • Website
  • Contact
Last update: January 2015

Responsible of diagnostic test


Somatic genetics

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region
Sanger sequencing

Additional information

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.