Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families

Approximately 1% of the global population is affected by intellectual disability (ID), and the majority receive no molecular diagnosis. Previous studies have indicated high levels of genetic heterogeneity, with estimates of more than 2500 autosomal ID genes, the majority of which are autosomal reces...

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Veröffentlicht in:Molecular psychiatry 2018-04, Vol.23 (4), p.973-984
Hauptverfasser: Harripaul, R, Vasli, N, Mikhailov, A, Rafiq, M A, Mittal, K, Windpassinger, C, Sheikh, T I, Noor, A, Mahmood, H, Downey, S, Johnson, M, Vleuten, K, Bell, L, Ilyas, M, Khan, F S, Khan, V, Moradi, M, Ayaz, M, Naeem, F, Heidari, A, Ahmed, I, Ghadami, S, Agha, Z, Zeinali, S, Qamar, R, Mozhdehipanah, H, John, P, Mir, A, Ansar, M, French, L, Ayub, M, Vincent, J B
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Sprache:eng
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