剥脱综合征的遗传关联研究确定了LOXL1的保护性罕见变异和5个新的易感性位点。
昂山素季(Aung T, Ozaki M,李MC, Schlotzer-Schrehardt U, Thorleifsson G,沟口健二T, Igo RP Jr Haripriya,威廉姆斯,Astakhov Y,或者AC,体细胞杂种KP, Nakano年代,Mori K, Abu-Amero K,豪泽米,李Z, Prakadeeswari G,贝利JNC, Cherecheanu美联社,康JH,纳尔逊年代,Hayashi K, Manabe SI, Kazama年代,Zarnowski T,井上K, Irkec M, Coca-Prados M, Sugiyama K, Jarvela我Schlottmann P, Lerner科幻,Lamari H, Nilgun Y, Bikbov M,公园KH、Cha SC, Yamashiro K, Zenteno JC,乔纳斯JB, Kumar RS佩雷拉SA陈容易,Kobakhidze N,乔治•R Vijaya L, T,爱德华DP,德胡安·马科斯L Pakravan M, Moghimi年代,Ideta R, Bach-Holm D, Kappelgaard P, Wirostko B,托马斯年代,加斯顿D, Bedard说K,格里尔王,杨Z,陈X,黄L,唱J,贾H,贾L,乔C, H,刘X,赵B,王YX,徐L, Leruez年代,Reynier P, Chichua G, Tabagari年代,Uebe年代,Zenkel M, Berner D, Mossbock G, Weisschuh N, Hoja U, Welge-Luessen UC,冲入C, Founti P, Chatzikyriakidou,帕帕斯T, Anastasopoulos E, Lambropoulos,戈什,马纳尔Shetty R, Porporato N,萨拉瓦南V, R, Shivkumar C, Kalpana N, Sarangapani年代,Kanavi先生,贝尼省,Yazdani年代,Lashay, Naderifar H, Khatibi N,有限元分析,Lavia C, Dallorto L,罗尔T, Frezzotti P, Paoli D, Salvi E, Manunta P, Mori Y,宫田康弘K, Higashide T, Chihara E, Ishiko年代,吉田,昭M,登Y,大桥T,樱井T, T,杉本Chuman H, Aihara M, Inatani M,宅一生M,后藤N,松田F, Yoshimura N, Ikeda Y,上野M, Sotozono C, Jeoung JW, Sagong M,公园KH、安J,Cruz-Aguilar M, Ezzouhairi SM, Rafei Chong YF, Ng XY,吴作栋SR,陈Y,勇VHK,汗,Olawoye OO, Ashaye AO, Ugbede我Onakoya, Kizor-Akaraiwe N, Teekhasaenee C, Suwan Y, Supakontanasan W, Okeke年代,Uche新泽西,Asimadu我,阿尤布H,说明F, Kosior-Jarecka E, Lukasik U, Lischinsky我,卡斯特罗V, Grossmann RP, Sunaric Megevand G,罗伊,Dervan E, Silke E,饶,刚刚P, Fornero P, Cuello O,施华尼D, Zompa T,米尔斯RA, Souzeau E,米切尔P,王JJ,休伊特啊,库特M, Crowston詹,Astakhov SY, Akopov EL,Emelyanov一,Vysochinskaya V,Kazakbaeva G,Fayzrakhmanov R,铝Obeidan SA,Owaidhah O,Aljasim LA,Chowbay B,富JN,公所RQ,辛KS,解Z,畅AWO,莫SQ,洙HM,陈XY,白振华SQ,Heng KK, Husain R, Ho SL, Hillmer AM, Cheng CY, Escudero-Domínguez FA, González-Sarmiento R, Martinon-Torres F, Salas A, Pathanapitoon K, Hansapinyo L, Wanichwecharugruang B, Kitnarong N, Sakuntabhai A, Nguyn HX, Nguyn GTT, Nguyn TV, Zenz W, Binder A, Klobassa DS, Hibberd ML, Davila S, Herms S, Nöthen MM, Moebus S, Rautenbach RM, Ziskind A, Carmichael TR, Ramsay M, Álvarez L, García M, González-Iglesias H, Rodríguez-Calvo PP, Fernández-Vega Cueto L, Oguz Ç, Tamcelik N, Atalay E, Batu B, Aktas D, Kasım B, Wilson MR, Coleman AL, Liu Y, Challa P, Herndon L, Kuchtey RW, Kuchtey J, Curtin K, Chaya CJ, Crandall A, Zangwill LM, Wong TY, Nakano M, Kinoshita S, den Hollander AI, Vesti E, Fingert JH, Lee RK, Sit AJ, Shingleton BJ, Wang N, Cusi D, Qamar R, Kraft P, Pericak-Vance MA, Raychaudhuri S, Heegaard S, Kivelä T, Reis A, Kruse FE, Weinreb RN, Pasquale LR, Haines JL, Thorsteinsdottir U, Jonasson F, Allingham RR, Milea D, Ritch R, Kubota T, Tashiro K, Vithana EN, Micheal S, Topouzis F, Craig JE, Dubina M, Sundaresan P, Stefansson K, Wiggs JL, Pasutto F, Khor CC.
昂等。作者:emelyanov一。
纳特遗传学。2017年7月; 49(7):993-1004。DOI:10.1038 / ng.3875。电子版2017年5月29日。
纳特遗传学。2017年。
结论:28553957
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