CUGC for pontocerebellar hypoplasia type 9 and spastic paraplegia-63
Ashley PL Marsh, Gaia Novarino, Paul J Lockhart, Richard J Leventer
European Journal of Human Genetics | NATURE PUBLISHING GROUP | Published : 2019
Awarded by EuroGentest2 (Unit 2: "Genetic testing as part of health care"), a Coordination Action under FP7
Awarded by NHMRC Career Development Fellowship
This work was supported by EuroGentest2 (Unit 2: "Genetic testing as part of health care"), a Coordination Action under FP7 (Grant Agreement Number 261469) and the European Society of Human Genetics. We acknowledge the participation of the patients and their families in these studies, as well as the generous financial support of the Lefroy and Handbury families. APLM was supported by an Australian Postgraduate Award. PJL is supported by an NHMRC Career Development Fellowship (GNT1032364). RJL is supported by a Melbourne Children's Clinician Scientist Fellowship.