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Novel mutations of TCIRG1 cause a malignant and mild phenotype of autosomal recessive osteopetrosis (ARO) in four Chinese families
PaperCitations, authors & open-access status
Novel mutations of TCIRG1 cause a malignant and mild phenotype of autosomal recessive osteopetrosis (ARO) in four Chinese families is a paper indexed in ScholarIQ from OpenAlex. ScholarIQ records 19 citations, 2017 year and bronze oa status.
19
Citations
2017
Year
bronze
OA Status