Truncating loss-of-function mutations of DISP1 contribute to holoprosencephaly-like microform features in humans.
Roessler E; Ma Y; Ouspenskaia MV; Lacbawan F; Bendavid C; Dubourg C; Beachy PA; Muenke M; Human Genetics, 2009, vol. 125, issue 4, p 393, ISSN 14321203. ISBN 14321203.

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