PPP1R16B is a Critical Gene in 20q11.2 Microdeletion Syndrome: Loss of Function Variant in PPP1R16B in a Girl with Multiple Congenital Anomalies.

Nirmala Sirisena, Paul Kruszka, Maximilian Muenke and Vajira H.W. Dissanayake.
23rd Human Genome Meeting held at Seoul, South Korea from 24th – 26th April 2019. Abstracted in the conference proceedings, p.16.
Publication year: 2019