Familial neurohypophyseal diabetes insipidus: an extremely rare report of a family with a nonsense mutation in the arginine vasopressin gene

MLA

Diogo Ramalho, et al. “Familial Neurohypophyseal Diabetes Insipidus: An Extremely Rare Report of a Family with a Nonsense Mutation in the Arginine Vasopressin Gene.” Endocrine Abstracts, May 2022. 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...........71370dcf99c170456bb5783de762f06d&authtype=sso&custid=ns315887.

APA

Diogo Ramalho, Joana Serra-Caetano, Rita Cardoso, Patricia Rosinha, Araujo Barbara Filipa, Ines Rua, Orlando Rodrigues, Isabel Dinis, & Alice Mirante. (2022). Familial neurohypophyseal diabetes insipidus: an extremely rare report of a family with a nonsense mutation in the arginine vasopressin gene. Endocrine Abstracts.

Chicago

Diogo Ramalho, Joana Serra-Caetano, Rita Cardoso, Patricia Rosinha, Araujo Barbara Filipa, Ines Rua, Orlando Rodrigues, Isabel Dinis, and Alice Mirante. 2022. “Familial Neurohypophyseal Diabetes Insipidus: An Extremely Rare Report of a Family with a Nonsense Mutation in the Arginine Vasopressin Gene.” Endocrine Abstracts, May. 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...........71370dcf99c170456bb5783de762f06d&authtype=sso&custid=ns315887.