A novel point mutation in the translation initiation codon of the pre-pro-vasopressin-neurophysin II gene : cosegregation with morphological abnormalities and clinical symptoms in autosomal dominant neurohypophyseal diabetes insipidus

• RUTISHAUSER J

収録刊行物

• J Clin Endocrinol Metab

  J Clin Endocrinol Metab 81 192-198, 1996

詳細情報

• CRID: 1571135650597636992
• NII論文ID: 10021266585
• データソース種別:
  • CiNii Articles