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Author/Creator Minks, Kelly Q.

1. Autosomal dominant mitochondrial membrane protein‐associated neurodegeneration (MPAN). Issue 7 (13th May 2019)

Authors:
Gregory, Allison; Lotia, Mitesh; Jeong, Suh Young; Fox, Rachel; Zhen, Dolly; Sanford, Lynn; Hamada, Jeff; Jahic, Amir; Beetz, Christian; Freed, Alison; Kurian, Manju A.; Cullup, Thomas; van der Weijden, Marlous C. M.; Nguyen, Vy; Setthavongsack, Naly; Garcia, Daphne; Krajbich, Victoria; Pham, Tha...
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 7:Issue 7(2019)
Page Start:
n/a
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. Expanding the neurodevelopmental phenotype of PURA syndrome. Issue 1 (17th November 2017)

Authors:
Lee, Bo Hoon; Reijnders, Margot R. F.; Abubakare, Oluwatobi; Tuttle, Emily; Lape, Brynn; Minks, Kelly Q.; Stodgell, Christopher; Bennetto, Loisa; Kwon, Jennifer; Fong, Chin‐To; Gripp, Karen W.; Marsh, Eric D.; Smith, Wendy E.; Huq, Ahm M.; Coury, Stephanie A.; Tan, Wen‐Hann; Solis, Orestes; Mehta...
Journal:
American journal of medical genetics
Issue:
Volume 176:Issue 1(2018)
Page Start:
56
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗