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Items: 5

1.

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

Identifiers:
BioSample: SAMEA6527628; SRA: ERS4292032
Organism:
Equus caballus
Accession:
SAMEA6527628
ID:
15965405
2.

Blood - Congenital stationary night blindness, CSNB - Patient 2

Identifiers:
BioSample: SAMN17256418; Sample name: CASEID_164; SRA: SRS7989563
Organism:
Homo sapiens
isolate: Congenital stationary night blindness, CSNB - Patient 2
Package:
Human; version 1.0
Accession:
SAMN17256418
ID:
17256418
3.

Blood - Congenital stationary night blindness, CSNB - Patient 1

Identifiers:
BioSample: SAMN17256362; Sample name: CASEID_104; SRA: SRS7989670
Organism:
Homo sapiens
isolate: Congenital stationary night blindness, CSNB - Patient 1
Package:
Human; version 1.0
Accession:
SAMN17256362
ID:
17256362
4.

Genomic DNA extracted from peripheral blood of a CSNB patient

Identifiers:
BioSample: SAMN31373058; Sample name: CSNB-2018-V5
Organism:
Homo sapiens
isolate: Han
Package:
Human; version 1.0
Accession:
SAMN31373058
ID:
31373058
5.

OMIA001486-9615 - Night blindness, congenital stationary, LRIT3-related in Canis lupus familiaris (dog) [9615]

Identifiers:
BioSample: SAMEA11349836; SRA: ERS8995039
Organism:
Canis lupus familiaris
Accession:
SAMEA11349836
ID:
23549986
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