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HARVARD Citation
Kaygusuz, E. et al. (2021). A 24‐generation‐old founder mutation impairs splicing of RBBP8 in Pakistani families affected with Jawad syndrome. Clinical genetics. 100 (4), pp. 486-488. [Online].
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Kaygusuz, E. et al. (2021). A 24‐generation‐old founder mutation impairs splicing of RBBP8 in Pakistani families affected with Jawad syndrome. Clinical genetics. 100 (4), pp. 486-488. [Online].