Dispelling myths about rare disease registry system development (vol 8, pg 21, 2013)

被引：2

作者：

Bellgard, Matthew ^{[1
]}

Beroud, Christophe ^{[2
,3
]}

Parkinson, Kay ^{[4
]}

Harris, Tess ^{[5
]}

Ayme, Segolene ^{[6
]}

Baynam, Gareth ^{[7
,8
,9
]}

Weeramanthri, Tarun ^{[10
]}

Dawkins, Hugh ^{[1
,10
,11
,12
]}

Hunter, Adam ^{[1
]}

机构：

[1] Murdoch Univ, Ctr Comparat Genom, Perth, WA 6150, Australia

[2] Aix Marseille Univ, INSERM UMR 910, Fac Med Timone, Marseille, France

[3] Hop Enfants La Timone, AP HM, Dept Genet Med, Marseille, HM, France

[4] Alstrom Syndrome, Paignton TQ3 1LH, Devon, England

[5] Polycyst Kidney Dis Char UK, PKD Int Ciliopathy Alliance, London, England

[6] INSERM US14, ORPHANET, F-75014 Paris, France

[7] King Edward Mem Hosp, Genet Serv Western Australia, Perth, WA, Australia

[8] Univ Western Australia, Sch Paediat & Child Hlth, Perth, WA, Australia

[9] Murdoch Univ, Inst Immunol & Infect Dis, Perth, WA, Australia

[10] Govt Western Australia, Dept Hlth, Publ Hlth & Clin Serv Div, Off Populat Hlth Genom, Perth, WA, Australia

[11] Univ Western Australia, Sch Pathol & Lab Med, Perth, WA, Australia

[12] Curtin Univ Technol, Curtin Hlth Innovat Res Inst, Perth, WA, Australia

来源：

基金：

英国医学研究理事会;

关键词：

D O I：

10.1186/1751-0473-9-4

中图分类号：

Q [生物科学];

学科分类号：

07 [理学]; 0710 [生物学]; 09 [农学];

摘要：

引用

页数：1