Associated Papers
Identification of novel mutation in RANKL by whole-exome sequencing in a Thai family with osteopetrosis; a case report and review of RANKL osteopetrosis.
Lertwilaiwittaya P et al.
Molecular Genetics & Genomic Medicine, 2021
RANKL cytokine: from pioneer of the osteoimmunology era to cure for a rare disease.
Lo Iacono N et al.
Clinical & Developmental Immunology, 2013
Osteoclast-poor human osteopetrosis due to mutations in the gene encoding RANKL.
Sobacchi C et al.
Nature Genetics, 2007
Select a paper to view details