Disorders of histone methylation: Molecular basis and clinical syndromes.

Al Ojaimi, Mode; Banimortada, Bashar J; Othman, Amna; Riedhammer, Korbinian M; Almannai, Mohammed; El-Hattab, Ayman W

Al Ojaimi, Mode; Banimortada, Bashar J; Othman, Amna; Riedhammer, Korbinian M; Almannai, Mohammed; El-Hattab, Ayman W.

Afiliación

Al Ojaimi M; College of Medicine, University of Sharjah, Sharjah, United Arab Emirates.
Banimortada BJ; Pediatrics Department, University Hospital Sharjah, Sharjah, United Arab Emirates.
Othman A; College of Medicine, University of Sharjah, Sharjah, United Arab Emirates.
Riedhammer KM; Department of Medical Genetics, Hamad Medical Corporation, Doha, Qatar.
Almannai M; Institute of Human Genetics, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, Munich, Germany.
El-Hattab AW; Department of Nephrology, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, Munich, Germany.

Clin Genet ; 102(3): 169-181, 2022 09.

Article en En | MEDLINE | ID: mdl-35713103

Asunto(s)

Histonas; Lisina; Histona Demetilasas/genética; Histona Metiltransferasas/metabolismo; N-Metiltransferasa de Histona-Lisina/genética; Histonas/genética; Histonas/metabolismo; Humanos; Lisina/química; Lisina/genética; Lisina/metabolismo; Metilación; Síndrome

Palabras clave

COMPASS; epigenetics; histone demethylases; histone methylation; histone methyltransferases; neurodevelopmental disorders

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Histonas / Lisina Límite: Humans Idioma: En Revista: Clin Genet Año: 2022 Tipo del documento: Article País de afiliación: Emiratos Árabes Unidos

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