S-EPMC12580737 - A Mild Ataxia-Dominant Phenotype of Phosphomannomutase 2-Congenital Disorder of Glycosylation in a Tunisian Family: Broadening the Geographical Scope. - OmicsDI

Unknown

Dataset Information

A Mild Ataxia-Dominant Phenotype of Phosphomannomutase 2-Congenital Disorder of Glycosylation in a Tunisian Family: Broadening the Geographical Scope.

ABSTRACT:

SUBMITTER: Zouari R

PROVIDER: S-EPMC12580737 | biostudies-literature | 2025 Oct

REPOSITORIES: biostudies-literature