Disease: Osteopetrosis- mild autosomal recessive form
- <em>CLCN7</em>-Related Osteopetrosis
- A mild autosomal recessive form of osteopetrosis
- A Mild Case of Autosomal Recessive Osteopetrosis Masquerading as the Dominant Form Involving Homozygous Deep Intronic Variations in the CLCN7 Gene
- CLCN7-Related Osteopetrosis
- Early and transient osteopetrosis in microphthalmic MIB-rats
- Fracture patterns in malignant osteopetrosis (Albers-Schonberg disease)
- Malignant Infantile Osteopetrosis
- Novel c.G630A TCIRG1 mutation causes aberrant splicing resulting in an unusually mild form of autosomal recessive osteopetrosis
- Novel mutations of CLCN7 cause autosomal dominant osteopetrosis type II (ADO-II) and intermediate autosomal recessive osteopetrosis (IARO) in Chinese patients
- Osteoclast-poor osteopetrosis
- Osteopetrosis associated with PLEKHM1 and SNX10 genes, both involved in osteoclast vesicular trafficking
- Osteopetrosis in children
- Osteopetrosis: further heterogeneity
- Osteopetrosis: genetics, treatment and new insights into osteoclast function
- Osteopetrotic induced pluripotent stem cells derived from patients with different disease-associated mutations by non-integrating reprogramming methods
- RANK receptor oligomerisation in the regulation of NFκB signalling
- RANK-dependent autosomal recessive osteopetrosis: characterization of five new cases with novel mutations
- Spectrum of Skeletal Imaging Features in Osteopetrosis: Inheritance Pattern and Radiological Associations
- Successful cord blood transplantation in a patient with malignant infantile osteopetrosis and hemophilia