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My child has been diagnosed with LCA. What do we need to do to participate in Project 3000?
Will insurance cover genetic testing for LCA?
I have learned that my insurance company will not pay for genetic testing. Now what?
Our child has been diagnosed with LCA. Why are we being asked for “parental” samples? Neither of us is affected.
What is the protocol for submitting parental samples?
What can I personally do to move research forward?
Articles of Interest:
Leber congenital amaurosis: Clinical correlations with genotypes, gene therapy trials update, and future directions.
Visual Acuity in Patients with Leber's Congenital Amaurosis and Early Childhood-Onset Retinitis Pigmentosa
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Last modified Sun, 03/15/2009 - 09:29
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