Tehran University of Medical Sciences Researchers Yield New Study Findings on Progressive Myoclonic Epilepsy (A case of a 6-year-old girl with a rare compound heterozygous mutation of KCTD7 presenting with progressive myoclonic epilepsy).

MLA

“Tehran University of Medical Sciences Researchers Yield New Study Findings on Progressive Myoclonic Epilepsy (A Case of a 6-Year-Old Girl with a Rare Compound Heterozygous Mutation of KCTD7 Presenting with Progressive Myoclonic Epilepsy).” Genomics & Genetics Weekly, Nov. 2024, p. 1859. EBSCOhost, widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edo&AN=181019584&authtype=sso&custid=ns315887.

APA

Tehran University of Medical Sciences Researchers Yield New Study Findings on Progressive Myoclonic Epilepsy (A case of a 6-year-old girl with a rare compound heterozygous mutation of KCTD7 presenting with progressive myoclonic epilepsy). (2024). Genomics & Genetics Weekly, 1859.

Chicago

“Tehran University of Medical Sciences Researchers Yield New Study Findings on Progressive Myoclonic Epilepsy (A Case of a 6-Year-Old Girl with a Rare Compound Heterozygous Mutation of KCTD7 Presenting with Progressive Myoclonic Epilepsy).” 2024. Genomics & Genetics Weekly, November, 1859. http://widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edo&AN=181019584&authtype=sso&custid=ns315887.