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10.1007/s00439-017-1779-6 http://scihub22266oqcxt.onion/10.1007/s00439-017-1779-6 C5429360!5429360 !28349240     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=28349240 &cmd=llinks): Failed to open stream: HTTP request failed! 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The Human Gene Mutation Database: towards a comprehensive repository of inherited mutation data for medical research, genetic diagnosis and next-generation sequencing studies |pdf=|usr=}}{{28349240 }} gab.com Text The Human Gene Mutation Database: towards a comprehensive repository of inherited mutation data for medical research, genetic diagnosis and next-generation sequencing studies JO: Hum Genet http://www.kidney.de/pget.php?&tw=1&pmid=28349240 #FOAvip The Human Gene Mutation Database (HGMD(®)) constitutes a comprehensive collection of published germline mutations in nuclear genes that underlie, or are closely associated with human inherited disease. At the time of writing (March 2017), the database contained in excess of 203,000 different gene lesions identified in over 8000 genes manually curated from over 2600 journals. With new mutation entries currently accumulating at a rate exceeding 17,000 per annum, HGMD represents de facto the central unified gene/disease-oriented repository of heritable mutations causing human genetic disease used worldwide by researchers, clinicians, diagnostic laboratories and genetic counsellors, and is an essential tool for the annotation of next-generation sequencing data. The public version of HGMD ( http://www.hgmd.org ) is freely available to registered users from academic institutions and non-profit organisations whilst the subscription version (HGMD Professional) is available to academic, clinical and commercial users under license via QIAGEN Inc. Twit Text FOAVip The Human Gene Mutation Database: towards a comprehensive repository of inherited mutation data for medical research, genetic diagnosis and next-generation sequencing studies ????Hum Genet http://www.kidney.de/pget.php?&tw=1&pmid=28349240 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28349240 #FOAvip English Wikipedia <ref>{{Cite pmid|28349240 }}</ref> The Human Gene Mutation Database: towards a comprehensive repository of inherited mutation data for medical research, genetic diagnosis and next-generation sequencing studies #MMPMID28349240 Stenson PD ; Mort M ; Ball EV ; Evans K ; Hayden M ; Heywood S ; Hussain M ; Phillips AD ; Cooper DN Hum Genet 2017[Jun]; 136 (6 ): 665-677 PMID28349240 show ga The Human Gene Mutation Database (HGMD(®)) constitutes a comprehensive collection of published germline mutations in nuclear genes that underlie, or are closely associated with human inherited disease. At the time of writing (March 2017), the database contained in excess of 203,000 different gene lesions identified in over 8000 genes manually curated from over 2600 journals. With new mutation entries currently accumulating at a rate exceeding 17,000 per annum, HGMD represents de facto the central unified gene/disease-oriented repository of heritable mutations causing human genetic disease used worldwide by researchers, clinicians, diagnostic laboratories and genetic counsellors, and is an essential tool for the annotation of next-generation sequencing data. The public version of HGMD ( http://www.hgmd.org ) is freely available to registered users from academic institutions and non-profit organisations whilst the subscription version (HGMD Professional) is available to academic, clinical and commercial users under license via QIAGEN Inc. |*Databases, Genetic [MESH] |*Mutation [MESH] |Humans [MESH]The Human Gene Mutation Database: towards a comprehensive repository o(epmc).pdf DeepDyve Pubget Overpricing