Constitutional SAMD9L mutations cause familial myelodysplastic syndrome and transient monosomy 7

Pastor, VB (author)

Sahoo, SS (author)

Boklan, J (author)

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Schwabe, GC (author)

Saribeyoglu, E (author)

Strahm, B (author)

Lebrecht, D (author)

Voss, M (author)

Karolinska Institutet

Bryceson, YT (author)

Karolinska Institutet

Erlacher, M (author)

Ehninger, G (author)

Niewisch, M (author)

Schlegelberger, B (author)

Baumann, I (author)

Achermann, JC (author)

Shimamura, A (author)

Hochrein, J (author)

Tedgard, U (author)

Nilsson, L (author)

Hasle, H (author)

Boerries, M (author)

Busch, H (author)

Niemeyer, CM (author)

Wlodarski, MW (author)

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 (creator_code:org_t)

2017-12-07

2018

English.

In: Haematologica. - : Ferrata Storti Foundation (Haematologica). - 1592-8721 .- 0390-6078. ; 103:3, s. 427-437

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• Journal article (peer-reviewed)