Homozygous IL37 Mutation Leads to Infantile Inflammatory Bowel Disease

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Platforms
dbGaP
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phs002040.v1.p1
APIs
dbGaP FHIR
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Consent Codes

GRU-IRB

Focus / Diseases

Inflammatory Bowel Diseases

Study Design

Family/Twin/Trios

Data Types

SNP/CNV Genotypes (NGS)

Subjects

3