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Nature Communications
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February 14, 2026
Loss-of-function variants in the CAPN1 activator CD99L2 cause X-linked spastic ataxia
Benita Menden, Rana D Incebacak Eltemur, German Demidov, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 20, 2026
Expanding the clinical spectrum of RNU4ATAC-opathies: more frequent and diverse than assumed
Silvestre Cuinat, Valérie Cormier-Daire, Jeremie Rosain, et al.
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Showing results (101-110 of 102) with videos related to
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Page
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This site can display upto 102 results.
Nature Communications
|
February 14, 2026
Loss-of-function variants in the CAPN1 activator CD99L2 cause X-linked spastic ataxia
Benita Menden, Rana D Incebacak Eltemur, German Demidov, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 20, 2026
Expanding the clinical spectrum of RNU4ATAC-opathies: more frequent and diverse than assumed
Silvestre Cuinat, Valérie Cormier-Daire, Jeremie Rosain, et al.
Page
of 11