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Results for “Mct8 (Slc16A2)-Specific Thyroid Hormone Cell Transporter Deficiency”

3 trials

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Showing 3 of 3 results

Not applicableStudy completedNCT02699190
What this trial is testing

LeukoSEQ: Whole Genome Sequencing as a First-Line Diagnostic Tool for Leukodystrophies

Who this might be right for
LeukodystrophyWhite Matter Disease4H Syndrome+61 more
Children's Hospital of Philadelphia 236
Not applicableAvailableNCT04143295
What this trial is testing

Rescue of Infants With MCT8 Deficiency

Who this might be right for
Mct8 (Slc16A2)-Specific Thyroid Hormone Cell Transporter Deficiency
Roy E. Weiss, M.D.
Not applicableLooking for participantsNCT03047369
What this trial is testing

The Myelin Disorders Biorepository Project

Who this might be right for
LeukodystrophyWhite Matter DiseaseLeukoencephalopathies+63 more
Children's Hospital of Philadelphia 12,000