Angelman syndrome and severe infections in a patient with de novo 15q11.2-q13.1 deletion and maternally inherited 2q21.3 microdeletion

Author:

Neubert, Gerda; von Au, Katja; Drossel, Katrin; Tzschach, Andreas; Horn, Denise; Nickel, Renate; Kaindl, Angela M.

Tübinger Autor(en):

Published in:

Gene (2013), Bd. 512, H. 2, S. 453-455

Verlagsangabe:

Elsevier Science Bv

Language:

English

Full text:

ISSN:

0378-1119

DDC Classifikation:

570 - Life sciences; biology
610 - Medicine and health

Dokumentart:

Article

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