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Clinical Genetics
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May 26, 2022
Biallelic variants in ZNF142 lead to a syndromic neurodevelopmental disorder
Maria B Christensen, Amanda M Levy, Nazanin A Mohammadi, et al.
Medrxiv : the Preprint Server for Health Sciences
|
August 16, 2024
<i>PSMF1</i> variants cause a phenotypic spectrum from early-onset Parkinson's disease to perinatal lethality by disrupting mitochondrial pathways
Francesca Magrinelli, Christelle Tesson, Plamena R Angelova, et al.
Nature Communications
|
April 15, 2026
Variants in the proteasome regulator PSMF1 cause a phenotypic spectrum from parkinsonism to perinatal lethality
Francesca Magrinelli, Christelle Tesson, Plamena R Angelova, et al.
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of 9
Search research articles
Search
Showing results (81-90 of 83) with videos related to
Sort By:
Page
of 9
You have reached the last page of results.
This site can display upto 83 results.
Clinical Genetics
|
May 26, 2022
Biallelic variants in ZNF142 lead to a syndromic neurodevelopmental disorder
Maria B Christensen, Amanda M Levy, Nazanin A Mohammadi, et al.
Medrxiv : the Preprint Server for Health Sciences
|
August 16, 2024
<i>PSMF1</i> variants cause a phenotypic spectrum from early-onset Parkinson's disease to perinatal lethality by disrupting mitochondrial pathways
Francesca Magrinelli, Christelle Tesson, Plamena R Angelova, et al.
Nature Communications
|
April 15, 2026
Variants in the proteasome regulator PSMF1 cause a phenotypic spectrum from parkinsonism to perinatal lethality
Francesca Magrinelli, Christelle Tesson, Plamena R Angelova, et al.
Page
of 9