Special Issue: Genetics of Prader-Willi Syndrome

David E Godler; Merlin G Butler

doi:10.3390/genes12091429

Special Issue: Genetics of Prader-Willi Syndrome

Genes (Basel). 2021 Sep 16;12(9):1429. doi: 10.3390/genes12091429.

Authors

David E Godler^{1

2}, Merlin G Butler³

Affiliations

¹ Royal Children's Hospital, Murdoch Children's Research Institute, Parkville 3052, Australia.
² Department of Paediatrics, University of Melbourne, Parkville 3052, Australia.
³ Departments of Psychiatry & Behavioral Sciences and Pediatrics, University of Kansas Medical Center, Kansas City, KS 66160, USA.

Abstract

This Special Issue includes 15 peer-reviewed articles for publication by experts in Prader-Willi syndrome (PWS) and their reflective area of interest impacting this rare disorder [...].

Publication types

Editorial
Introductory Journal Article
Research Support, Non-U.S. Gov't

MeSH terms

Databases, Genetic
Genetic Association Studies
Humans
Pharmacogenomic Testing
Phenotype
Prader-Willi Syndrome / diagnosis
Prader-Willi Syndrome / epidemiology
Prader-Willi Syndrome / genetics*
Prader-Willi Syndrome / therapy
Rare Diseases / epidemiology
Rare Diseases / genetics