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Andrew J Duncan

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American Journal of Human Genetics|December 3, 2014

Mutations in SNX14 cause a distinctive autosomal-recessive cerebellar ataxia and intellectual disability syndromeAnna C Thomas, Hywel Williams, Núria Setó-Salvia, et al.

Neurology(R) Neuroimmunology & Neuroinflammation|June 19, 2025

Acute and Long-Term Immune-Treatment Strategies in Anti-LGI1 Antibody-Mediated Encephalitis: A Multicenter Cohort StudyNabil Seery, Robb Wesselingh, Paul Beech, et al.

Human Molecular Genetics|January 27, 2018

Mutations involving the SRY-related gene SOX8 are associated with a spectrum of human reproductive anomaliesMarie-France Portnoi, Marie-Charlotte Dumargne, Sandra Rojo, et al.

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Search research articles

Showing results (41-50 of 43) with videos related to

Sort By:

Pageof 5

You have reached the last page of results.This site can display upto 43 results.

American Journal of Human Genetics|December 3, 2014

Mutations in SNX14 cause a distinctive autosomal-recessive cerebellar ataxia and intellectual disability syndromeAnna C Thomas, Hywel Williams, Núria Setó-Salvia, et al.

Neurology(R) Neuroimmunology & Neuroinflammation|June 19, 2025

Acute and Long-Term Immune-Treatment Strategies in Anti-LGI1 Antibody-Mediated Encephalitis: A Multicenter Cohort StudyNabil Seery, Robb Wesselingh, Paul Beech, et al.

Human Molecular Genetics|January 27, 2018

Mutations involving the SRY-related gene SOX8 are associated with a spectrum of human reproductive anomaliesMarie-France Portnoi, Marie-Charlotte Dumargne, Sandra Rojo, et al.

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