A Missense Mutation in the MBTPS2 Gene Underlies the X-Linked Form of Olmsted Syndrome

被引:42
|
作者
Haghighi, Alireza [1 ]
Scott, Claire A. [2 ]
Poon, Daniel S. [2 ]
Yaghoobi, Reza [3 ]
Saleh-Gohari, Nasrollah [4 ]
Plagnol, Vincent [5 ]
Kelsell, David P. [2 ]
机构
[1] Univ Oxford, Nuffield Dept Clin Med, Wellcome Trust Ctr Human Genet, Oxford, England
[2] Queen Mary Univ London, Barts & London Sch Med & Dent, Ctr Cutaneous Res, Blizard Inst, London, England
[3] Ahvaz Jundishapur Univ Med Sci, Dept Dermatol, Ahvaz, Iran
[4] Kerman Univ Med Sci, Dept Genet, Kerman, Iran
[5] UCL, Genet Inst, London, England
关键词
IFAP SYNDROME; CLEAVAGE; FOLLICULARIS; PROTEIN;
D O I
10.1038/jid.2012.289
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
引用
收藏
页码:571 / 573
页数:3
相关论文
共 50 条
  • [1] MBTPS2 Mutation Causes BRESEK/BRESHECK Syndrome
    Naiki, Misako
    Mizuno, Seiji
    Yamada, Kenichiro
    Yamada, Yasukazu
    Kimura, Reiko
    Oshiro, Makoto
    Okamoto, Nobuhiko
    Makita, Yoshio
    Seishima, Mariko
    Wakamatsu, Nobuaki
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2012, 158A (01) : 97 - 102
  • [2] MBTPS2 mutations cause defective regulated intramembrane proteolysis in X-linked osteogenesis imperfecta
    Lindert, Uschi
    Cabral, Wayne A.
    Ausavarat, Surasawadee
    Tongkobpetch, Siraprapa
    Ludin, Katja
    Barnes, Aileen M.
    Yeetong, Patra
    Weis, Maryann
    Krabichler, Birgit
    Srichomthong, Chalurmpon
    Makareeva, Elena N.
    Janecke, Andreas R.
    Leikin, Sergey
    Rothlisberger, Benno
    Rohrbach, Marianne
    Kennerknecht, Ingo
    Eyre, David R.
    Suphapeetiporn, Kanya
    Giunta, Cecilia
    Marini, Joan C.
    Shotelersuk, Vorasuk
    NATURE COMMUNICATIONS, 2016, 7
  • [3] MBTPS2 mutations cause defective regulated intramembrane proteolysis in X-linked osteogenesis imperfecta
    Uschi Lindert
    Wayne A. Cabral
    Surasawadee Ausavarat
    Siraprapa Tongkobpetch
    Katja Ludin
    Aileen M. Barnes
    Patra Yeetong
    Maryann Weis
    Birgit Krabichler
    Chalurmpon Srichomthong
    Elena N. Makareeva
    Andreas R. Janecke
    Sergey Leikin
    Benno Röthlisberger
    Marianne Rohrbach
    Ingo Kennerknecht
    David R. Eyre
    Kanya Suphapeetiporn
    Cecilia Giunta
    Joan C. Marini
    Vorasuk Shotelersuk
    Nature Communications, 7
  • [4] A novel missense mutation in the ectodysplasin-A (EDA) gene underlies X-linked recessive nonsyndromic hypodontia
    Ayub, Muhammad
    Ur-Rehman, Fazal
    Yasinzai, Masoom
    Ahmad, Wasim
    INTERNATIONAL JOURNAL OF DERMATOLOGY, 2010, 49 (12) : 1399 - 1402
  • [5] A Novel Mutation in the MBTPS2 Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome
    Shin, Jun-Oh
    Roh, Dongyoung
    Shin, Kihyuk
    Kim, Woo-Il
    Yang, Min-Young
    Lee, Won-Ku
    Kim, Hoon-Soo
    Kim, Byung-Soo
    Kim, Moon-Bum
    Ko, Hyun-Chang
    ANNALS OF DERMATOLOGY, 2022, 34 (01) : 59 - 62
  • [6] A recurrent missense mutation in the KAL gene in patients with X-linked Kallmann's syndrome
    Maya-Nuñez, G
    Zenteno, JC
    Ulloa-Aguirre, A
    Kofman-Alfaro, S
    Mendez, JP
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1998, 83 (05): : 1650 - 1653
  • [7] Recurrent splice-site mutation in MBTPS2 underlying IFAP syndrome with Olmsted syndrome-like features in a Chinese patient
    Wang, H. J.
    Tang, Z. L.
    Lin, Z. M.
    Dai, L. L.
    Chen, Q.
    Yang, Y.
    CLINICAL AND EXPERIMENTAL DERMATOLOGY, 2014, 39 (02) : 158 - 161
  • [8] A Japanese case of ichthyosis follicularis with atrichia and photophobia syndrome with an MBTPS2 mutation
    Junko Nakayama
    Nobuaki Iwasaki
    Kenji Shin
    Hideo Sato
    Mariko Kamo
    Manabu Ohyama
    Emiko Noguchi
    Tadao Arinami
    Journal of Human Genetics, 2011, 56 : 250 - 252
  • [9] A Japanese case of ichthyosis follicularis with atrichia and photophobia syndrome with an MBTPS2 mutation
    Nakayama, Junko
    Iwasaki, Nobuaki
    Shin, Kenji
    Sato, Hideo
    Kamo, Mariko
    Ohyama, Manabu
    Noguchi, Emiko
    Arinami, Tadao
    JOURNAL OF HUMAN GENETICS, 2011, 56 (03) : 250 - 252
  • [10] A novel mutation in MBTPS2 causes ichthyosis follicularis, alopecia, and photophobia syndrome
    Jiang, Yanyun
    Jin, Hongzhong
    Zeng, Yueping
    MOLECULAR GENETICS & GENOMIC MEDICINE, 2019, 7 (08):