Autosomal dominant osteopetrosis associated with renal tubular acidosis is due to a CLCN7 mutation.

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Piret, SE; Gorvin, CM; Trinh, A; Taylor, J; Lise, S; Taylor, JC; Ebeling, PR; Thakker, RVDate
2016-11Source Title
American Journal of Medical Genetics Part APublisher
WileyUniversity of Melbourne Author/s
Ebeling, PeterAffiliation
Melbourne Medical SchoolMetadata
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Journal ArticleCitations
Piret, S. E., Gorvin, C. M., Trinh, A., Taylor, J., Lise, S., Taylor, J. C., Ebeling, P. R. & Thakker, R. V. (2016). Autosomal dominant osteopetrosis associated with renal tubular acidosis is due to a CLCN7 mutation.. Am J Med Genet A, 170 (11), pp.2988-2992. https://doi.org/10.1002/ajmg.a.37755.Access Status
Open AccessOpen Access at PMC
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5132132Export Reference in RIS Format
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