Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localized enamel defects.

被引:0
|
作者
Hart, TC
Hart, PS
Gorry, MC
Michalec, MD
Ryu, O
Uygur, C
Ozdemir, D
Firatli, S
Aren, G
Firatli, E
机构
[1] Univ Pittsburgh, Sch Publ Hlth, Pittsburgh, PA 15260 USA
[2] Univ Istanbul, Sch Dent, Istanbul, Turkey
关键词
D O I
暂无
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
2283
引用
收藏
页码:558 / 558
页数:1
相关论文
共 50 条
  • [1] Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects
    Hart, TC
    Hart, PS
    Gorry, MC
    Michalec, MD
    Ryu, OH
    Uygur, C
    Ozdemir, D
    Firatli, S
    Aren, G
    Firatli, E
    JOURNAL OF MEDICAL GENETICS, 2003, 40 (12) : 900 - 906
  • [2] A novel ENAM mutation causes hypoplastic amelogenesis imperfecta
    Yu, Shunlan
    Zhang, Chenying
    Zhu, Ce
    Quan, Junkang
    Liu, Dandan
    Wang, Xiaozhe
    Zheng, Shuguo
    ORAL DISEASES, 2022, 28 (06) : 1610 - 1619
  • [3] Simple recessive mutation in ENAM is associated with amelogenesis imperfecta in Italian Greyhounds
    Gandolfi, Barbara
    Liu, Hongwei
    Griffioen, Layle
    Pedersen, Niels C.
    ANIMAL GENETICS, 2013, 44 (05) : 569 - 578
  • [4] Novel ITGB6 mutation in autosomal recessive amelogenesis imperfecta
    Seymen, F.
    Lee, K-E
    Koruyucu, M.
    Gencay, K.
    Bayram, M.
    Tuna, E. B.
    Lee, Z. H.
    Kim, J-W
    ORAL DISEASES, 2015, 21 (04) : 456 - 461
  • [5] Novel FAM20A mutation causes autosomal recessive amelogenesis imperfecta
    Volodarsky, Michael
    Zilberman, Uri
    Birk, Ohad S.
    ARCHIVES OF ORAL BIOLOGY, 2015, 60 (06) : 919 - 922
  • [6] The Structure and Composition of Deciduous Enamel Affected by Local Hypoplastic Autosomal Dominant Amelogenesis Imperfecta Resulting from an ENAM Mutation
    Shore, R. C.
    Backman, B.
    Elcock, C.
    Brook, A. H.
    Brookes, S. J.
    Kirkham, J.
    CELLS TISSUES ORGANS, 2010, 191 (04) : 301 - 306
  • [7] ENAM mutations in autosomal-dominant amelogenesis imperfecta
    Kim, JW
    Seymen, F
    Lin, BPJ
    Kiziltan, B
    Gencay, K
    Simmer, JP
    Hu, JCC
    JOURNAL OF DENTAL RESEARCH, 2005, 84 (03) : 278 - 282
  • [8] Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfecta
    Hart, PS
    Hart, TC
    Michalec, MD
    Ryu, OH
    Simmons, D
    Hong, S
    Wright, JT
    JOURNAL OF MEDICAL GENETICS, 2004, 41 (07) : 545 - 549
  • [9] MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfecta
    Kim, JW
    Simmer, JP
    Hart, TC
    Hart, PS
    Ramaswami, MD
    Bartlett, JD
    Hu, JCC
    JOURNAL OF MEDICAL GENETICS, 2005, 42 (03) : 271 - 275
  • [10] Mutations in RELT cause autosomal recessive amelogenesis imperfecta
    Kim, Jung-Wook
    Zhang, Hong
    Seymen, Figen
    Koruyucu, Mine
    Hu, Yuanyuan
    Kang, Jenny
    Kim, Youn J.
    Ikeda, Atsushi
    Kasimoglu, Yelda
    Bayram, Merve
    Zhang, Chuhua
    Kawasaki, Kazuhiko
    Bartlett, John D.
    Saunders, Thomas L.
    Simmer, James P.
    Hu, Jan C-C.
    CLINICAL GENETICS, 2019, 95 (03) : 375 - 383