Genetic heterogeneity of sarcoglycanopathies within a single Tunisian families

被引:0
|
作者
Fendri, K [1 ]
Amouri, R [1 ]
Kefi, M [1 ]
Hentati, F [1 ]
机构
[1] Natl Inst Neurol, Tunis, Tunisia
关键词
D O I
暂无
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
引用
收藏
页码:677 / 677
页数:1
相关论文
共 50 条
  • [21] Disclosure of Genetic Information Within Families
    Gallo, Agatha M.
    Angst, Denise B.
    Knafl, Kathleen A.
    AMERICAN JOURNAL OF NURSING, 2009, 109 (04) : 65 - 69
  • [22] PHENOTYPIC HETEROGENEITY WITHIN FAMILIES WITH ALZHEIMERS-DISEASE
    LOPEZ, R
    BARKER, W
    ZATINSKY, M
    GRAU, L
    DUARA, R
    NEUROLOGY, 1993, 43 (04) : A192 - A192
  • [23] FRDA and AVED patients within a single Tunisian family
    Amouri, Rim
    Zouari, Mourad
    Bouhlal, Yosr
    Eleuch, Ghada
    Ben Hamida, Christiane
    Hentati, Faycal
    NEUROMUSCULAR DISORDERS, 2006, 16 : S126 - S126
  • [24] Tunisian hereditary spastic paraplegias: clinical variability supported by genetic heterogeneity
    Boukhris, A.
    Stevanin, G.
    Feki, I.
    Denora, P.
    Elleuch, N.
    Miladi, M. I.
    Goizet, C.
    Truchetto, J.
    Belal, S.
    Brice, A.
    Mhiri, C.
    CLINICAL GENETICS, 2009, 75 (06) : 527 - 536
  • [25] Evidence for a genetic heterogeneity of megaloblastic anemia 1 in Tunisian patients.
    Bouchlaka, C
    Maktouf, C
    Sfar, T
    Ayadi, A
    M'kaour, A
    Sioud, M
    Gueddich, N
    Belhadjali, Z
    Dellagi, K
    Abdelhak, S
    AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (04) : 529 - 529
  • [26] Giant axonal neuropathy: clinical and genetic study in eight Tunisian families
    Kacem, A.
    Kefi, M.
    Amouri, R.
    Hentati, F.
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 2009, 285 : S143 - S143
  • [27] Ocular manifestations associated with nephronophthisis and genetic study in three Tunisian families
    Sellami, D.
    Makni, K.
    Chaker, H.
    Kharrat, M.
    Hentati, N.
    Kammoun, K.
    Chabouni, F.
    Ben Hamida, M.
    Hachicha, J.
    Salomon, R.
    Antignac, C.
    Ayadi, H.
    Feki, J.
    JOURNAL FRANCAIS D OPHTALMOLOGIE, 2006, 29 (09): : 1019 - 1023
  • [28] Genetic spectrum of sarcoglycanopathies in a cohort of Russian patients
    Bulakh, Maria
    Polyakova, Daria
    Dadali, Elena
    Rudenskaya, Galina
    Sharkova, Inna
    Markova, Tatiana
    Murtazina, Aysylu
    Demina, Nina
    Kurbatov, Sergei
    Nikitina, Natalia
    Udalova, Vasilisa
    Polyakov, Aleksander
    Ryzhkova, Oxana
    GENE, 2024, 927
  • [29] Genetic heterogeneity in Italian families with familial hemiplegic migraine
    Carrera, P
    Piatti, M
    Stenirri, S
    Grimaldi, LME
    Marchioni, E
    Curcio, M
    Righetti, PG
    Ferrari, M
    Gelfi, C
    NEUROLOGY, 1999, 53 (01) : 26 - 33
  • [30] GENETIC-HETEROGENEITY IN FAMILIES WITH HEREDITARY MULTIPLE EXOSTOSES
    COOK, A
    RASKIND, W
    BLANTON, SH
    PAULI, RM
    GREGG, RG
    FRANCOMANO, CA
    PUFFENBERGER, E
    CONRAD, EU
    SCHMALE, G
    SCHELLENBERG, G
    WIJSMAN, E
    HECHT, JT
    WELLS, D
    WAGNER, MJ
    AMERICAN JOURNAL OF HUMAN GENETICS, 1993, 53 (01) : 71 - 79