No abstract available

de Boer, E., Ockeloen, C.W., Matalonga, L., Horvath, R., Cohen, E., Cuesta, I., et al. (2021). Correction: A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis (European Journal of Human Genetics, (2021), 29, 9, (1359-1368), 10.1038/s41431-021-00900-2). EUROPEAN JOURNAL OF HUMAN GENETICS, 29(9), 1470-1471 [10.1038/s41431-021-00937-3].

Correction: A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis (European Journal of Human Genetics, (2021), 29, 9, (1359-1368), 10.1038/s41431-021-00900-2)

Benetti E.
Membro del Collaboration Group
;
Pinelli M.
Membro del Collaboration Group
;
Renieri A.
Membro del Collaboration Group
;
2021-01-01

Abstract

No abstract available
2021
de Boer, E., Ockeloen, C.W., Matalonga, L., Horvath, R., Cohen, E., Cuesta, I., et al. (2021). Correction: A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis (European Journal of Human Genetics, (2021), 29, 9, (1359-1368), 10.1038/s41431-021-00900-2). EUROPEAN JOURNAL OF HUMAN GENETICS, 29(9), 1470-1471 [10.1038/s41431-021-00937-3].
File in questo prodotto:
File Dimensione Formato  
Correction - A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis.pdf

non disponibili

Descrizione: Correction
Tipologia: PDF editoriale
Licenza: NON PUBBLICO - Accesso privato/ristretto
Dimensione 415.3 kB
Formato Adobe PDF
415.3 kB Adobe PDF   Visualizza/Apri   Richiedi una copia

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11365/1278557