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Paper Details

SNX10 gene mutation leading to osteopetrosis with dysfunctional osteoclasts.
Scientific Reports
35
2017
ARO, Autosomal recessive osteopetrosis, RANKL, S66Nfs, SNX10 gene, SNX10 transcript, Tonsillar herniation, anemia, c., dysfunctional, foramen magnum stenosis, intron 4, multinucleated osteoclasts, optic atrophy, osteoclast progenitors, osteoclasts, osteomyelitis of the jaw, osteopetrosis, patients, receptor activator of nuclear factor kappa-B ligand, sorting nexin 10
Author NameAffiliation
Göran HallmansUmea University
Adam AmeurUppsala University
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