Work

Neurobehavioral phenotype observed in KBG syndrome caused by ANKRD11 mutations.

Year: 2012

Type: article

Source: Archivio Istituzionale della Ricerca - Università degli Studi dell Aquila

Authors: Lo-Castro A, Brancati F, Digilio MC, Garaci FG, Bollero P, Alfieri P, Curatolo P.

Language: English

Topic: Genetics and Neurodevelopmental Disorders

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W7216814533

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