Recurrent mutations in the vasopressin-neurophysin II gene cause autosomal dominant neurohypophyseal diabetes insipidus.

D R Repaske; M L Summar; M R Krishnamani; E K Gültekin; M C Arriazu; M E Roubicek; M Blanco; G B Isaac; J A Phillips

doi:10.1210/jcem.81.6.8964872

Recurrent mutations in the vasopressin-neurophysin II gene cause autosomal dominant neurohypophyseal diabetes insipidus.

Identifier:nobleid.org/w1/20260515/3DFDC289

Type:Journal Article

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Recurrent mutations in the vasopressin-neurophysin II gene cause autosomal dominant neurohypophyseal diabetes insipidus.

Identifier:nobleid.org/w1/20260515/3DFDC289

Type:Journal Article

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