Ryan H Peretz
3PUBLICATIONS
1CO-AUTHORS
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Publications (3)
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|May 08, 2023
The remarkable journey of one female individual with ornithine transcarbamylase deficiency diagnosed post-mortem.RaeLynn Forsyth, Ryan H Peretz, Angela Dempsey
|Dec 21, 2022
A de novo hexokinase 1 (HK1) variant presenting as Boucher-Neuhäuser syndrome.Ryan H Peretz, Wadih M Zein, Robert B Hufnagel
|Mar 28, 2020
Natural history of the oldest known females with mucopolysaccharidosis type IVA (Morquio A syndrome).Ryan H Peretz, Christina H Flora, Darius J Adams
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