Items where authors include "Urquhart, JE"

Export as [feed] Atom [feed] RSS
Jump to: Article
Number of items: 1.

Article

Ratbi, I, Falkenberg, KD, Sommen, M et al. (28 more authors) (2015) Heimler Syndrome is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6. American Journal of Human Genetics, 97 (4). pp. 535-545. ISSN 0002-9297

This list was generated on Sun Jan 22 08:22:12 2023 GMT.