Neonatal presentation of occipital horn syndrome caused by a ATP7A missense variant
- PMID: 37114831
- DOI: 10.1002/jimd.12621
Neonatal presentation of occipital horn syndrome caused by a ATP7A missense variant
Comment on
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ATP7A-related copper transport disorders: A systematic review and definition of the clinical subtypes.J Inherit Metab Dis. 2023 Mar;46(2):163-173. doi: 10.1002/jimd.12590. Epub 2023 Feb 3. J Inherit Metab Dis. 2023. PMID: 36692329
References
REFERENCE
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- De Feyter S, Beyens A, Callewaert B. ATP7A-related copper transport disorders: A systematic review and definition of the clinical subtypes. J Inherit Metab Dis. 2023;46(2):163-173. doi:10.1002/jimd.12590.
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