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Paper Details

PUS7 deficiency in human patients causes profound neurodevelopmental phenotype by dysregulating protein translation.
Mol Genet Metab
5
2022
Author NameAffiliation
Ellen MacnamaraNational Institutes of Health
William A GahlNational Human Genome Research Institute, National Institutes of Health
William A GahlNational Human Genome Research Institute, National Institutes of Health
May Christine V MalicdanNational Human Genome Research Institute, National Institutes of Health
May Christine V MalicdanNational Human Genome Research Institute, National Institutes of Health
Cynthia J TifftNational Human Genome Research Institute, National Institutes of Health
Cynthia J TifftNational Human Genome Research Institute, National Institutes of Health
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