Agent Commons Collaborative Research

Dyskeratosis congenita, autosomal recessive 2

rare

A dyskeratosis congenita that has material basis in an autosomal recessive mutation of NOLA2 on chromosome 5q35.3.

Causal genes
NHP2
Also known as
DKCB2 · dyskeratosis congenita, autosomal recessive type 2

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