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Mutations in NGLY1 cause an inherited disorder of the endoplasmic reticulum-associated degradation pathway.
Genet Med. 2014 Oct;16(10):751-8. doi: 10.1038/gim.2014.22. Epub 2014 Mar 20.
Genet Med. 2014.
PMID: 24651605
Free PMC article.
Additional evidence that PGAP1 loss of function causes autosomal recessive global developmental delay and encephalopathy.
Williams C, Jiang YH, Shashi V, Crimian R, Schoch K, Harper A, McHale D, Goldstein D, Petrovski S.
Williams C, et al. Among authors: crimian r.
Clin Genet. 2015 Dec;88(6):597-9. doi: 10.1111/cge.12581. Epub 2015 Mar 30.
Clin Genet. 2015.
PMID: 25823418
No abstract available.
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Sustained therapeutic response to riboflavin in a child with a progressive neurological condition, diagnosed by whole-exome sequencing.
Shashi V, Petrovski S, Schoch K, Crimian R, Case LE, Khalid R, El-Dairi MA, Jiang YH, Mikati MA, Goldstein DB.
Shashi V, et al. Among authors: crimian r.
Cold Spring Harb Mol Case Stud. 2015 Oct;1(1):a000265. doi: 10.1101/mcs.a000265.
Cold Spring Harb Mol Case Stud. 2015.
PMID: 27148562
Free PMC article.
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Exome sequencing results in successful riboflavin treatment of a rapidly progressive neurological condition.
Petrovski S, Shashi V, Petrou S, Schoch K, McSweeney KM, Dhindsa RS, Krueger B, Crimian R, Case LE, Khalid R, El-Dairi MA, Jiang YH, Mikati MA, Goldstein DB.
Petrovski S, et al. Among authors: crimian r.
Cold Spring Harb Mol Case Stud. 2015 Oct;1(1):a000257. doi: 10.1101/mcs.a000257.
Cold Spring Harb Mol Case Stud. 2015.
PMID: 27148561
Free PMC article.
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