PRJNA673425 - Severe congenital neutropenia with syndromic features in a patient with homozygous hypomorphic DBF4 mutation - OmicsDI

Genomics

Dataset Information

Severe congenital neutropenia with syndromic features in a patient with homozygous hypomorphic DBF4 mutation

ABSTRACT: Severe congenital neutropenia with syndromic features in a patient with homozygous hypomorphic DBF4 mutation

PROVIDER: PRJNA673425 | ENA |

REPOSITORIES: ENA