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Article

Allgrove Syndrome and a Novel Mutation of AAAS Gene in a Boy.

Indian pediatrics - 15 Jan 2020

Gupta Saniya, Dayal Devi

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PMID: 31937715

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Related research

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Allgrove Syndrome and a Novel Mutation of AAAS Gene in a Boy.PMID 31937715Read ↗

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Neurological manifestations of Allgrove syndrome in patients carrying a potentially founder p.Ser263Pro variant in the AAAS gene.Semantic proximity Read ↗

Two cases of Allgrove syndrome with mutations in the AAAS gene.Semantic proximity Read ↗

Clinical and Genetic Characterization of 26 Tunisian Patients with Allgrove Syndrome.Semantic proximity Read ↗

[Allgrove syndrome in the mainland of China: clinical report and mutation analysis].Semantic proximity Read ↗

Neurological manifestations of Allgrove syndrome in patients carrying a potentially founder p.Ser263Pro variant of the AAAS geneSemantic proximity Read ↗

Clinical and genetic characterisation of a series of patients with triple A syndrome.Semantic proximity Read ↗

Analysis of the AAAS gene in a Japanese patient with triple A syndrome.Semantic proximity Read ↗

Allgrove Syndrome: A Report of New Pathological Variants in the AAAS Gene.Semantic proximity Read ↗

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