Literature DB >> 21548022

Significant liver disease in a patient with Y116H mutation in the MVK gene.

Melissa Leyva-Vega1, Pamela F Weiss, Jaya Ganesh, Laura Conlin, Nancy B Spinner, Randolph P Matthews.   

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Year:  2011        PMID： 21548022     DOI： 10.1002/ajmg.a.33915

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN： 1552-4825            Impact factor:   2.802


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  4 in total

1.  Evolution. Systematic humanization of yeast genes reveals conserved functions and genetic modularity.

Authors:  Aashiq H Kachroo; Jon M Laurent; Christopher M Yellman; Austin G Meyer; Claus O Wilke; Edward M Marcotte
Journal:  Science       Date:  2015-05-22       Impact factor: 47.728

2.  11-Month-Old Infant With Periodic Fevers, Recurrent Liver Dysfunction, and Perforin Gene Polymorphism.

Authors:  Grant S Schulert; Kevin Bove; Richard McMasters; Kathleen Campbell; Nancy Leslie; Alexei A Grom
Journal:  Arthritis Care Res (Hoboken)       Date:  2015-08       Impact factor: 4.794

3.  Neonatal hepatitis as first manifestation of hyperimmunoglobulinemia d syndrome.

Authors:  Marie-Louise von Linstow; Vibeke Rosenfeldt
Journal:  Case Rep Pediatr       Date:  2014-03-03

Review 4.  Natural history of mevalonate kinase deficiency: a literature review.

Authors:  Shumin Zhang
Journal:  Pediatr Rheumatol Online J       Date:  2016-05-04       Impact factor: 3.054
  4 in total

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