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Genetic and molecular basis of hematopoietic abnormalities in ZTTK syndrome

US National Heart Lung and Blood Institute grant open #nih-5R01HL168659-03

Summary

PROJECT SUMMARY Individuals with rare genetic diseases do not receive attention from the medical and research community. One out of two patients diagnosed with a rare disease is a child, meaning that patients and their families must endure long battles relating to disease progress throughout their child’s lifetime. Therefore, characterization of clinical/molecular aspects of rare diseases will greatly benefit young patients and their families. SON is a DNA- and RNA-binding protein that plays dual roles as an RNA splicing factor and a transcriptional repressor. Our research team recently identi

Genetic and molecular basis of hematopoiet…
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