Genomics

Dataset Information

0

Severe combined immunodeficiency with ligase 1 deficiency and Omenn-like manifestation


ABSTRACT: Searching the genetic cause in patient with SCID and Omenn-like phenotype

INSTRUMENT(S): Illumina

ORGANISM(S): Homo Sapiens

SUBMITTER: Medical University of Lodz 

PROVIDER: PRJEB56316 | EVA | 2022-09-30

REPOSITORIES: EVA

Dataset's files

Source:
Action DRS
SCID_LIG1_seq.vcf.csi Other
SCID_LIG1_seq.vcf.gz Vcf
SCID_LIG1_seq.vcf.gz.csi Vcf
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