ℹ️
🇬🇧
Search
Search for people relevant for "prevalence"
prevalence
Person
Class
Person
Publication
Programmes
Benjamin Cogné
Person without affiliation with CUNI
1 publication
Publication
publication
Rare germline heterozygous missense variants in BRCA1-associated protein 1, BAP1, cause a syndromic neurodevelopmental disorder
2022 |
Second Faculty of Medicine
Loading network view...
