News

Our New Website!

Welcome to our new website! We hope you find it more user friendly and full of important and useful features. Get to know us through photos of our group and writeups about our clinical and research activities.

New Tests

• CPT2 Gene Sequence Analysis
• Exercise Intolerance Mutation Profile + Expanded CPT2 Mutation Analysis
  • includes the most common mutations causing CPT II deficiency, McArdle disease and myoadenylate deaminase deficiency found in the “Exercise Intolerance Mutation Profile” plus  2 additional mutations from the “CPT2 Gene Mutation Profile” providing the most comprehensive  mutation screening we presently offer for exercise intolerance disorders.
• The Myoglobinuria Profile has been expanded to include myoadenylate deaminase analysis at a significantly reduced cost from that of the individual tests.

Research

A new section about our research activities provides a description of ongoing projects, information for potential participants, and required forms in a downloadable format. Information about our publications and related links are also included.

Contact Us

We invite you to write to us with questions or comments about our services.

Client Survey

We would appreciate your feedback about our services as well as any comments that would help us improve our services. - Survey