Biallelic variants in PIGN cause Fryns syndrome, multiple congenital anomalies-hypotonia-seizures syndrome, and neurologic phenotypes: A genotype–phenotype correlation study

MLA

Lucy Loong, et al. “Biallelic Variants in PIGN Cause Fryns Syndrome, Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome, and Neurologic Phenotypes: A Genotype–phenotype Correlation Study.” Genetics in Medicine, vol. 25, Jan. 2023, pp. 37–48. 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=edsair&AN=edsair.doi.dedup.....49e9de0ae400c9106d281bf224eddb14&authtype=sso&custid=ns315887.

APA

Lucy Loong, Agostina Tardivo, Alexej Knaus, Mona Hashim, Alistair T. Pagnamenta, Kerstin Alt, Helena Böhrer-Rabel, Alfonso Caro-Llopis, Trevor Cole, Felix Distelmaier, Patrick Edery, Carlos R. Ferreira, Aleksandra Jezela-Stanek, Bronwyn Kerr, Gerhard Kluger, Peter M. Krawitz, Marius Kuhn, Johannes R. Lemke, Gaetan Lesca, … Usha Kini. (2023). Biallelic variants in PIGN cause Fryns syndrome, multiple congenital anomalies-hypotonia-seizures syndrome, and neurologic phenotypes: A genotype–phenotype correlation study. Genetics in Medicine, 25, 37–48.

Chicago

Lucy Loong, Agostina Tardivo, Alexej Knaus, Mona Hashim, Alistair T. Pagnamenta, Kerstin Alt, Helena Böhrer-Rabel, et al. 2023. “Biallelic Variants in PIGN Cause Fryns Syndrome, Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome, and Neurologic Phenotypes: A Genotype–phenotype Correlation Study.” Genetics in Medicine 25 (January): 37–48. 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=edsair&AN=edsair.doi.dedup.....49e9de0ae400c9106d281bf224eddb14&authtype=sso&custid=ns315887.