Neuromuscular Disorders
Dystrophin gene and panel testing for Rare Neuromuscular Disorders (NMD) (germline DNA). This EQA has options for targeted DMD / BMD testing and/or NMD panel testing.
Prader-Willi and Angelman Syndromes (PW / AS)
Methylation and copy number analysis for Prader-Willi and Angelman Syndromes (PW / AS) (Germline DNA)
Spinocerebellar Ataxias (SCA)
Testing for Spinocerebellar Ataxias (SCA) (Germline DNA).
Huntington disease (HD)
HTT gene testing for Huntington disease (HD) (Germline DNA)
Cystic Fibrosis (CF)
CFTR testing for Cystic Fibrosis (germline DNA testing). To participate in EQA for Cystic Fibrosis, please go to our partner organisation’s (CF Network) website (https://eqascheme.org)