Using high throughput sequencing technologies to study genetic causes of ultra-rare neurological dis - detaljert visning

Using high throughput sequencing technologies to study genetic causes of ultra-rare neurological diseases

Waduwawatte Lekamalage Dulika Sanjeewani Sumathipala
Bok Engelsk 2022 · Doktoravhandlinger

Originaltittel	[ Using high throughput sequencing technologies to study genetic causes of ultra-rare neurological diseases ]

Opplysninger	Delvis opptrykk av artikler. - Årstall på tittelblad:. - Avhandling (Ph.D) - Universitetet i Oslo, 2021
Emner	Exome Sequencing : (DNLM)D000073359 Rare Diseases : (DNLM)D035583 Whole Exome Sequencing : (DNLM)D000073359
Sjanger	Doktoravhandlinger : https://id.nb.no/vocabulary/ntsf/61. - Doktoravhandlinger((uri)https://id.nb.no/vocabulary/ntsf/61) . - Doktoravhandlinger(https://id.nb.no/vocabulary/ntsf/61) ((NO-OsNB)ntsf61)
ISBN	8283779877. - 9788283779875