Associated Papers
Loss of EB2 delays mitotic progression in murine and human neural progenitors.
Phillips AW et al.
Development (cambridge, England), 2026
A de novo MAPRE2 variant in a patient with congenital symmetric circumferential skin creases type 2.
Feng J et al.
Molecular Genetics & Genomic Medicine, 2020
Intrafamiliar clinical variability of circumferential skin creases Kunze type caused by a novel heterozygous mutation of N-terminal TUBB gene.
Dentici ML et al.
Clinical Genetics, 2018
Mutations in Either TUBB or MAPRE2 Cause Circumferential Skin Creases Kunze Type.
Isrie M et al.
American Journal of Human Genetics, 2015
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