![Homozygous
<i>HOXB1</i>
loss-of-function mutation in a large family with hereditary congenital facial paresis]()
Homozygous
<i>HOXB1</i>
loss-of-function mutation in a large family with hereditary congenital facial paresisVogel, Markus; Velleuer, Eunike; Schmidt-Jiménez, Leon F.; Mayatepek, Ertan; Borkhardt, Arndt; Alawi, Malik; Kutsche, Kerstin; Kortüm, Fanny · American Journal of Medical Genetics Part A · 2016