Missense variants in DPYSL5 cause a neurodevelopmental disorder with corpus callosum agenesis and cerebellar abnormalities

Jeanne, M (author)

Demory, H (author)

Moutal, A (author)

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Vuillaume, ML (author)

Blesson, S (author)

Thepault, RA (author)

Marouillat, S (author)

Halewa, J (author)

Maas, SM (author)

Motazacker, MM (author)

Mancini, GMS (author)

Van Slegtenhorst, MA (author)

Andreou, A (author)

Cox, H (author)

Vogt, J (author)

Laufman, J (author)

Kostandyan, N (author)

Babikyan, D (author)

Hancarova, M (author)

Bendova, S (author)

Sedlacek, Z (author)

Aldinger, KA (author)

Sherr, EH (author)

Argilli, E (author)

England, EM (author)

Audebert-Bellanger, S (author)

Bonneau, D (author)

Colin, E (author)

Denomme-Pichon, AS (author)

Gilbert-Dussardier, B (author)

Isidor, B (author)

Kury, S (author)

Odent, S (author)

Redon, R (author)

Khanna, R (author)

Dobyns, WB (author)

Bezieau, S (author)

Honnorat, J (author)

Lohkamp, B (author)

Karolinska Institutet

Toutain, A (author)

Laumonnier, F (author)

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 (creator_code:org_t)

Elsevier BV, 2021

2021

English.

In: American journal of human genetics. - : Elsevier BV. - 1537-6605 .- 0002-9297. ; 108:5, s. 951-961

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• Journal article (peer-reviewed)