Homozygous IL37 mutation leads to infantile inflam... (ID 635708) - BioProject

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Accession: PRJNA635708 ID: 635708

Homozygous IL37 mutation leads to infantile inflammatory bowel disease (human)

See Genome Information for Homo sapiens

Whole-exome sequencing of a trio (parents and offspring) reveals IL37 mutation leads to infantile IBD.

Accession	PRJNA635708; dbGaP: phs002040
Type	Umbrella project (Subtype:Authorized Access)
Organism	Homo sapiens[Taxonomy ID: 9606] Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
Submission	Registration date: 28-May-2020 NIAID
Relevance	Medical

Project Data:

Resource Name	Number of Links
Genotype and Phenotype (dbGaP)	1

Homozygous IL37 mutation leads to infantile inflammatory bowel disease encompasses the following sub-project:

Project Type

Number of Projects

Phenotype or Genotype

BioProject accession	Organism	Title
PRJNA635709	Homo sapiens	Homozygous IL37 mutation leads to infantile inflammatory bowel disease (U.S. NATIONAL INST ALLERGY...)

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