Novel CLCN7 mutations cause autosomal dominant osteopetrosis type�II and intermediate autosomal recessive osteopetrosis

Title
Novel CLCN7 mutations cause autosomal dominant osteopetrosis type�II and intermediate autosomal recessive osteopetrosis
Authors
Keywords
-
Journal
Molecular Medicine Reports
Volume -, Issue -, Pages -
Publisher
Spandidos Publications
Online
2019-04-03
DOI
10.3892/mmr.2019.10123

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