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A novel splice site mutation of the arginine vasopressin–neurophysin II gene identified in a kindred with autosomal dominant familial neurohypophyseal diabetes insipidus

✍ Scribed by Hyun-Jung Tae; Ki-Hyun Baek; Sun-Mi Shim; Soon-Jib Yoo; Moo-Il Kang; Bong-Yun Cha; Kwang-Woo Lee; Ho-Young Son; Sung-Koo Kang


Book ID
116987657
Publisher
Elsevier Science
Year
2005
Tongue
English
Weight
339 KB
Volume
86
Category
Article
ISSN
1096-7192

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