Spectrum of Δ7-dehydrocholesterol reductase mutations in patients with the Smith-Lemli-Opitz (RSH) syndrome (Human Molecular Genetics (2000) vol.9 (1385-1391))

H. Yu, M. H. Lee, L. Starch, E. R. Elias, M. Irons, G. Salen, S. B. Patel, G. S. Tint

Research output: Contribution to journalComment/debatepeer-review

Original languageEnglish (US)
Pages (from-to)1903
Number of pages1
JournalHuman molecular genetics
Issue number12
StatePublished - 2000
Externally publishedYes

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Genetics(clinical)

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