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DiscussionWhat are the options for diagnosing mitochondrial disease?
Brain & Nervous System | Last Active: Jun 3 12:07am | Replies (6)Comment receiving replies
Replies to "Hi @JustinMcClanahan, No, I strictly did WGS through Nebula on my own because of my family..."
Go to the UMDF web page . That's the United mitochondrial disease foundation and they have all kinds of information that will help you. I have found they have more information than anywhere else. They are also very responsive and helpful if you reach out to them. They are also working with CHOP and have created a database for people who have or is suspected of having mito to register to help in studying this disease.