Data Collection Program Endorsement from Dr Nicole Wolf

Dr Nicole Wolf, 4H Leukodystrophy specialist and rare disease expert, stresses the importance of data collection, also called patient registries, and how critical it is for patients, caregivers, doctors and researchers to engage with them.

You can participate in the 4H Leukodystrophy by visiting the Data Collection Program here – https://4hleukodystrophy.rare-x.org/

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Data Collection Program Endorsement from Dr Nicole Wolf

Posted Under: Video

4H Leukodystrophy Research

4H Leukodystrophy
Research