Search Results - "Jurgensen, Taryn J" :: K.UTB vyhledávací portál

Variable phenotypes in congenital central hypoventilation syndrome with PHOX2B nonpolyalanine repeat mutations

by Kasi, Ajay S, Li, Hong, Jurgensen, Taryn J, Guglani, Lokesh, Keens, Thomas G, Perez, Iris A
Published in Journal of clinical sleep medicine (01.10.2021)

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Three-Generation Family With Congenital Central Hypoventilation Syndrome and Novel PHOX2B Gene Non-Polyalanine Repeat Mutation

by Kasi, Ajay S, Jurgensen, Taryn J, Yen, Stephanie, Kun, Sheila S, Keens, Thomas G, Perez, Iris A
Published in Journal of clinical sleep medicine (15.07.2017)

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Journal Article

Variable phenotypes in congenital central hypoventilation syndrome with PHOX2B nonpolyalanine repeat mutations

Three-Generation Family With Congenital Central Hypoventilation Syndrome and Novel PHOX2B Gene Non-Polyalanine Repeat Mutation

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