前のページに戻る この文献は全文を取り寄せることができます
JDreamⅢ複写サービスから文献全文の複写（冊子体のコピー）をお申込みできます。
ご利用には、G-Searchデータベースサービスまたは、JDreamⅢのIDが必要です。
既に、G-Searchデータベースサービスまたは、JDreamⅢのIDをお持ちの方
JDreamⅢ複写サービス
文献複写のお申込み
JDreamⅢ複写サービスのご利用が初めての方
学術文献の全文複写をお取寄せ
JDreamⅢ複写サービスのご案内
取り寄せる文献のタイトルと詳細
文献
J-GLOBAL ID：200902222287698830   整理番号：09A0854601

早期発症高尿酸血症,貧血および慢性腎不全に関連した優勢レニン遺伝子変異

Dominant Renin Gene Mutations Associated with Early-Onset Hyperuricemia, Anemia, and Chronic Kidney Failure
著者 (40件)：
ZIVNA Martina
(Center for Applied Genomics, Charles Univ. in Prague, First Fac. of Medicine, Prague 12000, CZE)
, 
ZIVNA Martina
(Inst. for Inherited Metabolic Disorders, Charles Univ. in Prague, First Fac. of Medicine, Prague 12000, CZE)
, 
HULKOVA Helena
(Inst. for Inherited Metabolic Disorders, Charles Univ. in Prague, First Fac. of Medicine, Prague 12000, CZE)
, 
MATIGNON Marie
(Assistance Publique-Hopitaux de Paris (AP-HP), Nephrology and Transplantation Unit, Henri Mondor Hospital, Creteil ...)
, 
MATIGNON Marie
(Paris XII Univ., Creteil 94010, FRA)
, 
HODANOVA Katerina
(Center for Applied Genomics, Charles Univ. in Prague, First Fac. of Medicine, Prague 12000, CZE)
, 
HODANOVA Katerina
(Inst. for Inherited Metabolic Disorders, Charles Univ. in Prague, First Fac. of Medicine, Prague 12000, CZE)
, 
VYLET’AL Petr
(Center for Applied Genomics, Charles Univ. in Prague, First Fac. of Medicine, Prague 12000, CZE)
, 
VYLET’AL Petr
(Inst. for Inherited Metabolic Disorders, Charles Univ. in Prague, First Fac. of Medicine, Prague 12000, CZE)
, 
KALBACOVA Marie
(Center for Applied Genomics, Charles Univ. in Prague, First Fac. of Medicine, Prague 12000, CZE)
, 
KALBACOVA Marie
(Inst. for Inherited Metabolic Disorders, Charles Univ. in Prague, First Fac. of Medicine, Prague 12000, CZE)
, 
BARESOVA Veronika
(Center for Applied Genomics, Charles Univ. in Prague, First Fac. of Medicine, Prague 12000, CZE)
, 
BARESOVA Veronika
(Inst. for Inherited Metabolic Disorders, Charles Univ. in Prague, First Fac. of Medicine, Prague 12000, CZE)
, 
SIKORA Jakub
(Inst. for Inherited Metabolic Disorders, Charles Univ. in Prague, First Fac. of Medicine, Prague 12000, CZE)
, 
BLAZKOVA Hana
(Inst. for Inherited Metabolic Disorders, Charles Univ. in Prague, First Fac. of Medicine, Prague 12000, CZE)
, 
ZIVNY Jan
(Inst. of Pathophysiology, Charles Univ. in Prague, First Fac. of Medicine, Prague 12000, CZE)
, 
IVANEK Robert
(Center for Applied Genomics, Charles Univ. in Prague, First Fac. of Medicine, Prague 12000, CZE)
, 
IVANEK Robert
(Inst. for Inherited Metabolic Disorders, Charles Univ. in Prague, First Fac. of Medicine, Prague 12000, CZE)
, 
STRANECKY Viktor
(Center for Applied Genomics, Charles Univ. in Prague, First Fac. of Medicine, Prague 12000, CZE)
, 
STRANECKY Viktor
(Inst. for Inherited Metabolic Disorders, Charles Univ. in Prague, First Fac. of Medicine, Prague 12000, CZE)
, 
SOVOVA Jana
(Inst. for Inherited Metabolic Disorders, Charles Univ. in Prague, First Fac. of Medicine, Prague 12000, CZE)
, 
CLAES Kathleen
(Dep. of Nephrology, Univ. Hospital Gasthuisberg, Leuven 3000, BEL)
, 
LERUT Evelyne
(Dep. of Nephrology, Univ. Hospital Gasthuisberg, Leuven 3000, BEL)
, 
FRYNS Jean-pierre
(Center for Human Genetics, Univ. of Leuven, Leuven 3000, BEL)
, 
HART P. Suzanne
(Office of the Clinical Director, National Human Genome Res. Inst., National Institutes of Health, Bethesda, MD ...)
, 
HART Thomas C.
(Human Craniofacial Genetics Section, National Inst. of Dental and Craniofacial Res., National Institutes of Health ...)
, 
ADAMS Jeremy N.
(Office of the Clinical Director, National Human Genome Res. Inst., National Institutes of Health, Bethesda, MD ...)
, 
PAWTOWSKI Audrey
(Assistance Publique-Hopitaux de Paris (AP-HP), Dep. de Genetique, Hopital Necker-Enfants Malades, Paris 75015, FRA)
, 
CLEMESSY Maud
(INSERM U833, Coll. de France, Paris 75005, FRA)
, 
GASC Jean-marie
(INSERM U833, Coll. de France, Paris 75005, FRA)
, 
GUEBLER Marie-claire
(INSERM U574, Hopital Necker-Enfants Malades, Paris 75015, FRA)
, 
GUEBLER Marie-claire
(Univ. Paris Descartes, Fac. de Medecine, Paris 75006, FRA)
, 
ANTIGNAC Corinne
(Assistance Publique-Hopitaux de Paris (AP-HP), Dep. de Genetique, Hopital Necker-Enfants Malades, Paris 75015, FRA)
, 
ANTIGNAC Corinne
(INSERM U574, Hopital Necker-Enfants Malades, Paris 75015, FRA)
, 
ANTIGNAC Corinne
(Univ. Paris Descartes, Fac. de Medecine, Paris 75006, FRA)
, 
ELLEDER Milan
(Center for Applied Genomics, Charles Univ. in Prague, First Fac. of Medicine, Prague 12000, CZE)
, 
ELLEDER Milan
(Inst. for Inherited Metabolic Disorders, Charles Univ. in Prague, First Fac. of Medicine, Prague 12000, CZE)
, 
KAPP Katja
(ZMBH (Center for Molecular Biology Heidelberg), Univ. of Heidelberg, Heidelberg D-69120, DEU)
, 
GRIMBERT Philippe
(Assistance Publique-Hopitaux de Paris (AP-HP), Nephrology and Transplantation Unit, Henri Mondor Hospital, Creteil ...)
, 
GRIMBERT Philippe
(Paris XII Univ., Creteil 94010, FRA)

資料名：
American Journal of Human Genetics  (American Journal of Human Genetics)

巻： 85  号： 2  ページ： 204-213  発行年： 2009年08月14日 
JST資料番号： B0360B  ISSN： 0002-9297  資料種別： 逐次刊行物 (A)
発行国： オランダ (NLD)  言語： 英語 (EN)
JDreamⅢ複写サービスとは
JDreamⅢ複写サービスは、学術文献の全文を複写（コピー）して取り寄せできる有料サービスです。インターネットに公開されていない文献や、図書館に収録されていない文献の全文を、オンラインで取り寄せることができます。J-GLOBALの整理番号にも対応しているので、申し込みも簡単にできます。全文の複写（コピー）は郵送またはFAXでお送りします

※ご利用には、G-Searchデータベースサービスまたは、JDreamⅢのIDが必要です
※初めてご利用される方は、JDreamⅢ複写サービスのご案内をご覧ください。

Copyright (c) 2009 Japan Science and Technology Agency. All Rights Reserved

TOP

BOTTOM