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Biochemical and cellular analysis of Ogden syndrome reveals downstream Nt-acetylation defects
Myklebust LM,
Van Damme P,
Stove SI,
Dorfel MJ,
Abboud A,
Kalvik TV,
Grauffel C,
Jonckheere V,
Wu Y,
Swensen J,
Kaasa H,
Liszczak G,
Marmorstein R,
Reuter N,
Lyon GJ,
Gevaert K,
Arnesen T

Human Molecular Genetics
  (0): Dec 8 2014   Nlm
[Abstract]
[DOI] [Full Text]

Erratum: Using VAAST to identify an X-linked disorder resulting in lethality in male infants due to N-terminal acetyltransferase deficiency (American Journal of Human Genetics (2011) 89 (28-43))
Rope AF,
Wang K,
Evjenth R,
Xing J,
Johnston JJ,
Swensen JJ,
Johnson WE,
Moore B,
Huff CD,
Bird LM,
Carey JC,
Opitz JM,
Stevens CA,
Jiang T,
Schank C,
Fain HD,
Robison R,
Dalley B,
Chin S,
South ST,
Pysher TJ,
Jorde LB,
Hakonarson H,
Lillehaug JR,
Biesecker LG,
Yandell M,
Arnesen T,
Lyon GJ

Am J Hum Genet
  89 (2): 345; Aug 12 2011  
[DOI]


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