Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains

Geisheker, MR (author)

Heymann, G (author)

Wang, TY (author)

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Coe, BP (author)

Turner, TN (author)

Stessman, HAF (author)

Hoekzema, K (author)

Kvarnung, M (author)

Karolinska Institutet

Shaw, M (author)

Friend, K (author)

Liebelt, J (author)

Barnett, C (author)

Thompson, EM (author)

Haan, E (author)

Guo, H (author)

Anderlid, BM (author)

Karolinska Institutet

Nordgren, A (author)

Karolinska Institutet

Lindstrand, A (author)

Karolinska Institutet

Vandeweyer, G (author)

Alberti, A (author)

Avola, E (author)

Vinci, M (author)

Giusto, S (author)

Pramparo, T (author)

Pierce, K (author)

Nalabolu, S (author)

Michaelson, JJ (author)

Sedlacek, Z (author)

Santen, GWE (author)

Peeters, H (author)

Hakonarson, H (author)

Courchesne, E (author)

Romano, C (author)

Kooy, RF (author)

Bernier, RA (author)

Nordenskjold, M (author)

Karolinska Institutet

Gecz, J (author)

Xia, K (author)

Zweifel, LS (author)

Eichler, EE (author)

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 (creator_code:org_t)

2017-06-19

2017

English.

In: Nature neuroscience. - : Springer Science and Business Media LLC. - 1546-1726 .- 1097-6256. ; 20:8, s. 1043-

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• Journal article (peer-reviewed)