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Paper Details

ATP6V1H Deficiency Impairs Bone Development through Activation of MMP9 and MMP13.
PLoS Genet
36
2017
ATP6V1H, ATP6V1H Deficiency, MMP13, MMP9, V-ATPase, V-ATPases, atp6v1h, atp6v1h mutants, bone loss, genetic disease, human, mature calcified bone cells, mmp13, mmp9, mutant atp6v1h, osteoporosis, patients, short stature, vacuolar ATPase, zebrafish
Author NameAffiliation
Valerie MaduroNIH and National Human Genome Research Institute
Valerie MaduroNIH and National Human Genome Research Institute
Camilo ToroNIH and National Human Genome Research Institute
Cornelius F BoerkoelNIH and National Human Genome Research Institute
Cornelius F BoerkoelNIH and National Human Genome Research Institute
William A GahlNational Human Genome Research Institute
William A GahlOffice of the Clinical Director, National Human Genome Research Institute/NIH
William A GahlNIH and National Human Genome Research Institute
William A GahlNational Human Genome Research Institute
William A GahlNIH and National Human Genome Research Institute
William A GahlOffice of the Clinical Director, National Human Genome Research Institute/NIH
May Christine V MalicdanNational Human Genome Research Institute
May Christine V MalicdanNIH and National Human Genome Research Institute
May Christine V MalicdanOffice of the Clinical Director, National Human Genome Research Institute/NIH
May Christine V MalicdanNational Human Genome Research Institute
May Christine V MalicdanNIH and National Human Genome Research Institute
May Christine V MalicdanOffice of the Clinical Director, National Human Genome Research Institute/NIH
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