Prader–Willi syndrome and early-onset morbid obesity NIH rare disease consortium: A review of natural history study

Merlin G. Butler, Virginia Kimonis, Elisabeth Dykens, June A. Gold, Jennifer Miller, Roy Tamura, Daniel J. Driscoll

Research output: Contribution to journalArticlepeer-review

Original languageEnglish
Pages (from-to)368-375
Number of pages8
JournalAmerican Journal of Medical Genetics, Part A
Volume176
Issue number2
DOIs
StatePublished - Feb 2018

ASJC Scopus Subject Areas

  • Genetics
  • Genetics(clinical)

Keywords

  • PWS genetic subtypes
  • Prader–Willi syndrome
  • genotype–phenotype correlations
  • longitudinal natural history study
  • mortality
  • rare disease consortium

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