Bone manifestations in Snyder‐Robinson syndrome

Author:

Koerner Teri L.,Green Armon M.,Pace-Farr Daniel J.,Zeitler Colton M.,Schwartz Matthew B.,Kutler Mary Jo F.

Publisher

Elsevier BV

Reference18 articles.

1. X-linked spermine synthase gene (SMS) defect: the first polyamine deficiency syndrome;Cason;Eur. J. Hum. Genet.: EJHG,2003

2. Impaired osteoblast and osteoclast function characterize the osteoporosis of Snyder - Robinson syndrome;Albert;Orphanet J. Rare Dis.,2015

3. Schwartz C.E., Peron A., Kutler M.J. Snyder-Robinson Syndrome. 〈www.ncbi.nlm.nih.gov〉. Published February 13, 2020. Accessed July 19, 2023. 〈https://www.ncbi.nlm.nih.gov/sites/books/NBK144284/〉.

4. Recessive SEx-linked Mental Retardation in the Absence of Other Recognizable Abnormalities;Snyder;Clin. Pediatr.,1969

5. Modeling snyder-robinson syndrome in multipotent stromal cells reveals impaired mitochondrial function as a potential cause for deficient osteogenesis;Ramsay;Sci. Rep.,2019

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