Mutations of AKT3 are associated with a wide spectrum of developmental disorders including extreme megalencephaly

Alcantara, D (author)

Timms, AE (author)

Gripp, K (author)

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Baker, L (author)

Park, K (author)

Collins, S (author)

Cheng, C (author)

Stewart, F (author)

Mehta, SG (author)

Saggar, A (author)

Sztriha, L (author)

Zombor, M (author)

Caluseriu, O (author)

Mesterman, R (author)

Van Allen, MI (author)

Jacquinet, A (author)

Ygberg, S (author)

Karolinska Institutet

Bernstein, JA (author)

Wenger, AM (author)

Guturu, H (author)

Bejerano, G (author)

Gomez-Ospina, N (author)

Lehman, A (author)

Alfei, E (author)

Pantaleoni, C (author)

Conti, V (author)

Guerrini, R (author)

Moog, U (author)

Graham, JM (author)

Hevner, R (author)

Dobyns, WB (author)

O'Driscoll, M (author)

Mirzaa, GM (author)

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 (creator_code:org_t)

2017-09-07

2017

English.

In: Brain : a journal of neurology. - : Oxford University Press (OUP). - 1460-2156. ; 140:10, s. 2610-2622

Related links:

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• Journal article (peer-reviewed)