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2023 | 2 |
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Exome Analysis Reveals Novel Missense and Deletion Variants in the CC2D2A Gene as Causative of Joubert Syndrome.
Genes (Basel). 2023 Mar 28;14(4):810. doi: 10.3390/genes14040810.
Genes (Basel). 2023.
PMID: 37107568
Free PMC article.
Supratentorial Demyelinating Lesions Following Severe Acute Respiratory Syndrome Coronavirus-2 Infection: A Pediatric Case Report.
Boeri S, Martinez Popple M, Giacomini T, Bellini T, Severino M, Rossi A, Debbia C, Ancona S, Aldera E, Nobili L, Siri L.
Boeri S, et al. Among authors: martinez popple m.
Neuropediatrics. 2023 Feb;54(1):73-77. doi: 10.1055/s-0042-1757710. Epub 2022 Dec 23.
Neuropediatrics. 2023.
PMID: 36564023
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