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
来源：
NEUROMUSCULAR DISORDERS | 2005年 / 15卷 / 9-10期
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
  • [41] Genetic screening of two Tunisian families with generalized epilepsy with febrile seizures plus
    Fendri-Kriaa, N.
    Kammoun, F.
    Rebai, A.
    Kolsi, D.
    Salem, I. Hadj
    Fakhfakh, F.
    Triki, C.
    EUROPEAN JOURNAL OF NEUROLOGY, 2009, 16 (06) : 697 - 704
  • [42] Genetic analysis of 9 Tunisian families with constitutional clotting factor XI deficiency
    Kacem, S.
    Megdiche, F.
    Maalej, S.
    Frikha, R.
    Ghorbel, M.
    Kassar, O.
    Mbarek, L.
    Elloumi, M.
    Kamoun, H.
    Kallel, C.
    HAEMOPHILIA, 2019, 25 : 165 - 165
  • [43] Linkage analysis of three genetic loci for disease susceptibility in Tunisian Psoriatic families
    Ammar, M.
    Bouchlaka-Souissi, C.
    Rebai, A.
    Doss, N.
    Sioud, A.
    Zaraa, I.
    Dhaoui, R.
    Laamouri, R.
    Osman, A. Ben
    Ben Ammar-El Gaaied, A.
    Mokni, M.
    JOURNAL OF DERMATOLOGICAL SCIENCE, 2009, 54 (02) : 137 - 139
  • [44] Genetic heterogeneity in Hispanic families with autosomal dominant juvenile glaucoma
    WuDunn, D
    Parish, RK
    Inana, G
    OPHTHALMIC GENETICS, 1996, 17 (03): : 87 - 94
  • [45] GENETIC-HETEROGENEITY IN 22 FAMILIES WITH LONG QT SYNDROME
    TOWBIN, JA
    SIU, B
    ROBINSON, J
    MOSS, A
    AYYAGARI, R
    HEJTMANCIK, JF
    AMERICAN JOURNAL OF HUMAN GENETICS, 1993, 53 (03) : 1092 - 1092
  • [46] Genetic heterogeneity in epilepsy and comorbidities: insights from Pakistani families
    Yasin, Muhammad
    Licchetta, Laura
    Khan, Niamat
    Ullah, Irfan
    Jan, Zakir
    Dawood, Muhammad
    Ahmed, Asif Naveed
    Azeem, Arfa
    Minardi, Raffaella
    Carelli, Valerio
    Saleha, Shamim
    BMC NEUROLOGY, 2024, 24 (01)
  • [47] Genetic heterogeneity and HOMOG analysis in British malignant hyperthermia families
    Robinson, R
    Curran, JL
    Hall, WJ
    Halsall, PJ
    Hopkins, PM
    Markham, AF
    Stewart, AD
    West, SP
    Ellis, FR
    JOURNAL OF MEDICAL GENETICS, 1998, 35 (03) : 196 - 201
  • [48] Genetic professionals' reports of nondisclosure of genetic risk information within families
    Clarke, A
    Richards, M
    Kerzin-Storrar, L
    Halliday, J
    Young, MA
    Simpson, SA
    Featherstone, K
    Forrest, K
    Lucassen, A
    Morrison, PJ
    Quarrell, OWJ
    Stewart, H
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2005, 13 (05) : 556 - 562
  • [49] Genetic professionals' reports of nondisclosure of genetic risk information within families
    Angus Clarke
    Martin Richards
    Lauren Kerzin-Storrar
    Jane Halliday
    Mary Anne Young
    Sheila A Simpson
    Katie Featherstone
    Karen Forrest
    Anneke Lucassen
    Patrick J Morrison
    Oliver W J Quarrell
    Helen Stewart
    European Journal of Human Genetics, 2005, 13 : 556 - 562
  • [50] BIOCHEMICAL-CHARACTERIZATION OF PROPIONYL COA CARBOXYLASE DEFICIENCY - HETEROGENEITY WITHIN A SINGLE GENETIC COMPLEMENTATION GROUP
    MCKEON, C
    EANES, RZ
    WOLF, B
    BIOCHEMICAL GENETICS, 1982, 20 (1-2) : 77 - 94
12345