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Showing results (61-70 of 64) with videos related to

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American Journal of Human Genetics|June 8, 2019
Truncating Mutations in UBAP1 Cause Hereditary Spastic ParaplegiaMohammad Ali Farazi Fard, Adriana P Rebelo, Elena Buglo, et al.
American Journal of Human Genetics|April 2, 2019
Truncating Mutations in UBAP1 Cause Hereditary Spastic ParaplegiaMohammad Ali Farazi Fard, Adriana P Rebelo, Elena Buglo, et al.
Nature Genetics|May 28, 2020
Author Correction: Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetesAndrea Cortese, Yi Zhu, Adriana P Rebelo, et al.
Nature Genetics|May 6, 2020
Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetesAndrea Cortese, Yi Zhu, Adriana P Rebelo, et al.
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Showing results (61-70 of 64) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 64 results.
American Journal of Human Genetics|June 8, 2019
Truncating Mutations in UBAP1 Cause Hereditary Spastic ParaplegiaMohammad Ali Farazi Fard, Adriana P Rebelo, Elena Buglo, et al.
American Journal of Human Genetics|April 2, 2019
Truncating Mutations in UBAP1 Cause Hereditary Spastic ParaplegiaMohammad Ali Farazi Fard, Adriana P Rebelo, Elena Buglo, et al.
Nature Genetics|May 28, 2020
Author Correction: Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetesAndrea Cortese, Yi Zhu, Adriana P Rebelo, et al.
Nature Genetics|May 6, 2020
Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetesAndrea Cortese, Yi Zhu, Adriana P Rebelo, et al.
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