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Year | Number of Results |
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2020 | 1 |
2023 | 1 |
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Page 1
Quantitative MRI-Based Analysis Identifies Developmental Limbic Abnormalities in PCDH19 Encephalopathy.
Cereb Cortex. 2020 Oct 1;30(11):6039-6050. doi: 10.1093/cercor/bhaa177.
Cereb Cortex. 2020.
PMID: 32582916
Exome Analysis Reveals Novel Missense and Deletion Variants in the CC2D2A Gene as Causative of Joubert Syndrome.
Cabrita Pinto RL, Viaggi S, Canale E, Martinez Popple M, Capra V, Conteduca G, Testa B, Coviello D, Covone AE.
Cabrita Pinto RL, et al. Among authors: canale e.
Genes (Basel). 2023 Mar 28;14(4):810. doi: 10.3390/genes14040810.
Genes (Basel). 2023.
PMID: 37107568
Free PMC article.
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