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Items: 3

1.

Deep mutational scan to study the plasma membrane expression of 123 pathogenic rhodopsin variants

Project data type: Raw sequence reads
Scope:
Multispecies
Indiana University
Accession:
PRJNA817609
ID:
817609
2.

Whole Genome Sequencing Identifies Missense Mutation in GRM6 as the Likely Cause of Congenital Stationary Night Blindness in a Tennessee Walking Horse

Project data type: Other
Scope:
Monoisolate
UNIVERSITY OF CALIFORNIA - DAVIS
Accession:
PRJEB36381
ID:
660999
3.

Homo sapiens

Genome wide gene expression in a patient with 15q13.3 homozygous microdeletion syndrome

Taxonomy:
Homo sapiens (human)
Project data type: Transcriptome or Gene expression
Scope:
Multiisolate
Developmental genomics, Genetics research, Childrens Mercy Hospital
Accession:
PRJNA186785
ID:
186785

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