Heterozygous mutations in the ADCK3 gene in siblings with cerebellar atrophy and extreme phenotypic variability

Lubov Blumkin, Esther Leshinsky-Silver, Ayelet Zerem, Keren Yosovich, Tally Lerman-Sagie, Dorit Lev*

*Corresponding author for this work

Research output: Chapter in Book/Report/Conference proceedingChapterpeer-review

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Medicine & Life Sciences

Chemistry