A 24‐generation‐old founder mutation impairs splicing of RBBP8 in Pakistani families affected with Jawad syndrome.
- Resource Type
- Article
- Source
Clinical Genetics . Oct2021, Vol. 100 Issue 4, p486-488. 3p.- Subject
- *
PAKISTANIS
*FAMILIES
*KNOTS & splices
*SYNDROMES
*PHENOTYPIC plasticity - Language
- ISSN
- 0009-9163