Innovative Genome Joint Analysis for identification of novel deep-intronic de novo pathogenic variants in KMT2A gene - WiedemannSteiner Syndrom
- Resource Type
- Source
- Liječnički vjesnik
Volume 145
Issue Supp 2 - Subject
Hypertrichosis cubiti KMT2A protein, human Rare Disease Whole Genome Sequencing - Language
- English
- ISSN
- 1849-2177
0024-3477