2015
DOI: 10.1530/boneabs.4.p163
|View full text |Cite
|
Sign up to set email alerts
|

Whole blood gene expression analysis in idiopathic infantile hypercalcemia due to compound heterozygous mutation in theCYP24A1gene in an Austrian 4-month-old boy and his family

Help me understand this report

This publication either has no citations yet, or we are still processing them

Set email alert for when this publication receives citations?

See others like this or search for similar articles