Endocrinological features and epileptic encephalopathy in COX deficiency due to SCO1 mutations: case series and review of literature.
Barbato A, Gori G, Sacchini M, Pochiero F, Bargiacchi S, Traficante G, Palazzo V, Tiberi L, Bianchini C, Mei D, Parrini E, Pisano T, Procopio E, Guerrini R, Peron A, Stagi S.
Barbato A, et al. Among authors: bianchini c.
Endocr Connect. 2024 Aug 1:EC-24-0221. doi: 10.1530/EC-24-0221. Online ahead of print.
Endocr Connect. 2024.
PMID: 39214134
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