Mutations in the mitochondrial gene C12ORF65 lead to syndromic autosomal recessive intellectual disability and show genotype phenotype correlation

✍ Scribed by Buchert, Rebecca; Uebe, Steffen; Radwan, Farah; Tawamie, Hasan; Issa, Shaher; Shimazaki, Haruo; Henneke, Marco; Ekici, Arif B.; Reis, André; Abou Jamra, Rami

• Book ID: 123109081
• Publisher: Elsevier Science
• Year: 2013
• Tongue: English
• Weight: 785 KB
• Volume: 56
• Category: Article
• ISSN: 1769-7212
• DOI: 10.1016/j.ejmg.2013.09.010