Publication | Closed Access
A family with osteoporosis pseudoglioma syndrome due to compound heterozygosity of two novel mutations in the LRP5 gene
42
Citations
33
References
2006
Year
Mendelian DisorderGenetic DisorderGeneticsNovel MutationsPathologyOsteoporosis Pseudoglioma SyndromeOsteoporosisMedicineLrp5 Gene
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