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10.1002/acn3.229 http://scihub22266oqcxt.onion/10.1002/acn3.229 C4603380!4603380!26478897     free     free     free Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Ann+Clin+Transl+Neurol 2015 ; 2 (10): 972-7 Nephropedia Template TP {{tp|p=26478897|t=2015. Fine mapping of chromosome 15q25 implicates ZNF592 in neurosarcoidosis patients |pdf=|usr=}}{{26478897}} gab.com Text Fine mapping of chromosome 15q25 implicates ZNF592 in neurosarcoidosis patients JO: Ann Clin Transl Neurol http://www.kidney.de/pget.php?&tw=1&pmid=26478897 #FOAvip Neurosarcoidosis is a clinical subtype of sarcoidosis characterized by the presence of granulomas in the nervous system. Here, we report a highly significant association with a variant (rs75652600, P = 3.12 × 10?8, odds ratios = 4.34) within a zinc finger gene, ZNF592, from an imputation-based fine-mapping study of the chromosomal region 15q25 in African-Americans with neurosarcoidosis. We validate the association with ZNF592, a gene previously shown to cause cerebellar ataxia, in a cohort of European-Americans with neurosarcoidosis by uncovering low-frequency variants with a similar risk effect size (chr15:85309284, P = 0.0021, odds ratios = 5.36). Twit Text FOAVip Fine mapping of chromosome 15q25 implicates ZNF592 in neurosarcoidosis patients ????Ann Clin Transl Neurol http://www.kidney.de/pget.php?&tw=1&pmid=26478897 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26478897 #FOAvip English Wikipedia <ref>{{Cite pmid|26478897}}</ref> Fine mapping of chromosome 15q25 implicates ZNF592 in neurosarcoidosis patients #MMPMID26478897 Lareau CA; Adrianto I; Levin AM; Iannuzzi MC; Rybicki BA; Montgomery CG Ann Clin Transl Neurol 2015[Oct]; 2 (10): 972-7 PMID26478897show ga Neurosarcoidosis is a clinical subtype of sarcoidosis characterized by the presence of granulomas in the nervous system. Here, we report a highly significant association with a variant (rs75652600, P = 3.12 × 10?8, odds ratios = 4.34) within a zinc finger gene, ZNF592, from an imputation-based fine-mapping study of the chromosomal region 15q25 in African-Americans with neurosarcoidosis. We validate the association with ZNF592, a gene previously shown to cause cerebellar ataxia, in a cohort of European-Americans with neurosarcoidosis by uncovering low-frequency variants with a similar risk effect size (chr15:85309284, P = 0.0021, odds ratios = 5.36). äFine mapping of chromosome 15q25 implicates ZNF592 in neurosarcoidosis(epmc).pdf DeepDyve Pubget Overpricing