Published in
Wiley, Birth Defects Research, 7(110), p. 587-597, 2018
DOI: 10.1002/bdr2.1200
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Exome sequencing in syndromic brain malformations identifies novel mutations in ACTB, and SLC9A6, and suggests BAZ1A as a new candidate gene
Journal article published in 2018 by
Valerie Weitensteiner,
Rong Zhang,
Julia Bungenberg,
Matthias Marks,
Jan Gehlen,
Damian J. Ralser,
Alina C. Hilger,
Amit Sharma,
Johannes Schumacher,
Ulrich Gembruch 
,
Waltraut M. Merz,
Albert Becker,
Janine Altmüller ,
Holger Thiele,
Bernhard G. Herrmann
and other authors.
,
Waltraut M. Merz,
Albert Becker,
Janine Altmüller ,
Holger Thiele,
Bernhard G. Herrmann
and other authors.
This paper is made freely available by the publisher.
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