Author

L. Nosková

1 paper indexed here

Fetches their full publication history.

Not the right person? Other researchers publish under this name.

Open access Jun 2026

A role for EHMT2 in an autosomal recessive neurodevelopmental disorder is supported and anticipatory guidance for the patient’s family is allowed.

D. Rots, B. C. D. de Oliveira, L. M. L. Carvalho et al. · Frontiers in Genetics · 0 citations