Correspondence on "Pathogenic variants in USP7 cause a neurodevelopmental disorder with speech delays, altered behavior, and neurologic anomalies" by Fountain et al.

Capra, Anna Paola; Agolini, Emanuele; La Rosa, Maria Angela; Novelli, Antonio; Briuglia, Silvana

Capra, Anna Paola; Agolini, Emanuele; La Rosa, Maria Angela; Novelli, Antonio; Briuglia, Silvana.

Afiliación

Capra AP; Department of Biomedical, Dental, Morphological and Functional Imaging Sciences, University of Messina, Messina, Italy.
Agolini E; Laboratory of Medical Genetics, Bambino Gesù Children's Hospital, Rome, Italy.
La Rosa MA; Department of Biomedical, Dental, Morphological and Functional Imaging Sciences, University of Messina, Messina, Italy.
Novelli A; Laboratory of Medical Genetics, Bambino Gesù Children's Hospital, Rome, Italy.
Briuglia S; Department of Biomedical, Dental, Morphological and Functional Imaging Sciences, University of Messina, Messina, Italy. sbriuglia@unime.it.

Genet Med ; 23(2): 421-422, 2021 02.

Article en En | MEDLINE | ID: mdl-33012787

Asunto(s)

Trastornos del Desarrollo del Lenguaje; Trastornos del Neurodesarrollo; Humanos; Trastornos del Neurodesarrollo/genética; Peptidasa Específica de Ubiquitina 7

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trastornos del Neurodesarrollo / Trastornos del Desarrollo del Lenguaje Límite: Humans Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2021 Tipo del documento: Article País de afiliación: Italia

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