znf9 gene
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AB0779 Eosinophilic myositis and rheumatoid arthritis as first manifestation in a patient carrying myotonic dystrophy type 2 (CCTG)n expenssion of ZNF9 gene

Annals of the Rheumatic Diseases ◽

10.1136/annrheumdis-2012-eular.779 ◽

2013 ◽

Vol 71 (Suppl 3) ◽

pp. 683.3-683

Author(s):

A. Meyer ◽

A. Theulin ◽

E. Chatelus ◽

C. Sordet ◽

R.-M. Javier ◽

...

Keyword(s):

Rheumatoid Arthritis ◽

Myotonic Dystrophy ◽

Myotonic Dystrophy Type ◽

Myotonic Dystrophy Type 2 ◽

Znf9 Gene

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Myotonia congenita and myotonic dystrophy in the same family: coexistence of a CLCN1 mutation and expansion in the CNBP (ZNF9) gene

Clinical Genetics ◽

10.1111/j.1399-0004.2010.01616.x ◽

2011 ◽

Vol 80 (6) ◽

pp. 574-580 ◽

Cited By ~ 15

Author(s):

C Sun ◽

M Van Ghelue ◽

L Tranebjaerg ◽

F Thyssen ◽

Ø Nilssen ◽

...

Keyword(s):

Myotonic Dystrophy ◽

Myotonia Congenita ◽

Clcn1 Mutation ◽

Znf9 Gene

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Characterization of a single nucleotide polymorphism in the ZNF9 gene and analysis of association with myotonic dystrophy type II (DM2) in the Italian population

Molecular and Cellular Probes ◽

10.1016/j.mcp.2004.09.003 ◽

2005 ◽

Vol 19 (1) ◽

pp. 71-74 ◽

Cited By ~ 2

Author(s):

L. Vallo ◽

E. Bonifazi ◽

P. Borgiani ◽

G. Novelli ◽

A. Botta

Keyword(s):

Single Nucleotide Polymorphism ◽

Myotonic Dystrophy ◽

Italian Population ◽

Type Ii ◽

Myotonic Dystrophy Type ◽

Nucleotide Polymorphism ◽

Single Nucleotide ◽

Znf9 Gene

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An expansion in the ZNF9 gene causes PROMM in a previously described family with an incidental CLCN1 mutation

Journal of Neurology Neurosurgery & Psychiatry ◽

10.1136/jnnp.2003.018432 ◽

2004 ◽

Vol 75 (2) ◽

pp. 343-343 ◽

Cited By ~ 22

Author(s):

P J Lamont

Keyword(s):

Clcn1 Mutation ◽

Znf9 Gene

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