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10.4103/aian.AIAN_1130_20 http://scihub22266oqcxt.onion/10.4103/aian.AIAN_1130_20 35002148!8680880!35002148     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=35002148&cmd=llinks): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 215       Ann+Indian+Acad+Neurol 2021 ; 24 (5): 781-783 Nephropedia Template TP {{tp|p=35002148|t=2021. CNNM2 Heterozygous Variant Presenting as Hypomagnesemia and West Syndrome: Expanding the Spectrum of CNNM2 Gene-Related Epileptic Disorders |pdf=|usr=}}{{35002148}} gab.com Text CNNM2 Heterozygous Variant Presenting as Hypomagnesemia and West Syndrome: Expanding the Spectrum of CNNM2 Gene-Related Epileptic Disorders JO: Ann Indian Acad Neurol http://www.kidney.de/pget.php?&tw=1&pmid=35002148 #FOAvip ? Twit Text FOAVip CNNM2 Heterozygous Variant Presenting as Hypomagnesemia and West Syndrome: Expanding the Spectrum of CNNM2 Gene-Related Epileptic Disorders ????Ann Indian Acad Neurol http://www.kidney.de/pget.php?&tw=1&pmid=35002148 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=35002148 #FOAvip English Wikipedia <ref>{{Cite pmid|35002148}}</ref> CNNM2 Heterozygous Variant Presenting as Hypomagnesemia and West Syndrome: Expanding the Spectrum of CNNM2 Gene-Related Epileptic Disorders #MMPMID35002148 Panda PK; Lourembam R; Sharawat IK Ann Indian Acad Neurol 2021[Sep]; 24 (5): 781-783 PMID35002148show ga ? ?CNNM2 Heterozygous Variant Presenting as Hypomagnesemia and West Syndr(epmc).pdf DeepDyve Pubget Overpricing