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Page 1
Spectrum of ERCC6-Related Cockayne Syndrome (Type B): From Mild to Severe Forms.
Genes (Basel). 2024 Apr 18;15(4):508. doi: 10.3390/genes15040508.
Genes (Basel). 2024.
PMID: 38674442
Free PMC article.
PTCHD1 gene mutation/deletion: the cognitive-behavioral phenotyping of four case reports.
Montanaro FAM, Mandarino A, Alesi V, Schwartz C, Sepulveda DJC, Skinner C, Friez M, Piccolo G, Novelli A, Zanni G, Dentici ML, Vicari S, Alfieri P.
Montanaro FAM, et al. Among authors: piccolo g.
Front Psychiatry. 2024 Jan 15;14:1327802. doi: 10.3389/fpsyt.2023.1327802. eCollection 2023.
Front Psychiatry. 2024.
PMID: 38288059
Free PMC article.
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Corrigendum: PTCHD1 gene mutation/deletion: the cognitive-behavioral phenotyping of four case reports.
Montanaro FAM, Mandarino A, Alesi V, Schwartz C, Sepulveda DJC, Skinner C, Friez M, Piccolo G, Novelli A, Zanni G, Dentici ML, Vicari S, Alfieri P.
Montanaro FAM, et al. Among authors: piccolo g.
Front Psychiatry. 2024 Feb 13;15:1375954. doi: 10.3389/fpsyt.2024.1375954. eCollection 2024.
Front Psychiatry. 2024.
PMID: 38414498
Free PMC article.
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