A 3.2 Mb deletion on 18q12 in a patient with childhood autism and high-grade myopia

Autism spectrum disorders (ASDs) are a heterogeneous group of disorders with unknown aetiology. Even though ASDs are suggested to be among the most heritable complex disorders, only a few reproducible mutations leading to susceptibility for ASD have been identified. In an attempt to identify ASD sus...

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Bibliographic Details
Main Author: Gilling, M (author)
Other Authors: Lauritsen, MB (author), Møller, M (author), Henriksen, KF (author), Vicente, A (author), Oliveira, G (author), Cintin, C (author), Eiberg, H (author), Andersen, PS (author), Mors, O (author), Rosenberg, T (author), Brøndum-Nielsen, K (author), Cotterill, RM (author), Lundsteen, C (author), Ropers, HH (author), Ullmann, R (author), Bache, I (author), Tümer, Z (author), Tommerup, N (author)
Format: article
Language:eng
Published: 2012
Subjects:
Perturbação Autística
Miopia
Cromossoma Humano Par 18
Online Access:http://hdl.handle.net/10400.4/1382
Country:Portugal
Oai:oai:rihuc.huc.min-saude.pt:10400.4/1382

Internet

http://hdl.handle.net/10400.4/1382

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