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Search Results - CHKILI, Taieb
Search Results - CHKILI, Taieb
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A Novel GDAP1 Mutation P78L Responsible for CMT4A Disease in Three Moroccan Families
by
Bouhouche, Ahmed
,
Birouk, Nazha
,
Benomar, Ali
,
Ouazzani, Reda
,
Chkili, Taïeb
,
Yahyaoui, Mohamed
Published in
Canadian journal of neurological sciences
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A PCR Amplification Method Reveals Instability of the Dodecamer Repeat in Progressive Myoclonus Epilepsy (EPM1) and No Correlation between the Size of the Repeat and Age at Onset
by
Lalioti, Maria D.
,
Scott, Hamish S.
,
Genton, Pierre
,
Grid, Djamel
,
Ouazzani, Réda
,
M'Rabet, Amel
,
Ibrahim, Sadi
,
Gouider, Riadh
,
Dravet, Charlotte
,
Chkili, Taieb
,
Bottani, Armand
,
Buresi, Catherine
,
Malafosse, Alain
,
Antonarakis, Stylianos E.
Published in
American journal of human genetics
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Haplotype study of West European and North African Unverricht-Lundborg chromosomes: evidence for a few founder mutations
by
MOULARD, Bruno
,
GENTON, Pierre
,
UTERMANN, Barbara
,
BALDY-MOULINIER, Michel
,
BELAIDI, Halima
,
BERTRAN, Francoise
,
BIRABEN, Arnaud
,
CHERIF, André Ali
,
CHKILI, Taieb
,
CRESPEL, Arielle
,
DARCEL, Francoise
,
DULAC, Olivier
,
GRID, Djamel
,
GENY, Christian
,
HUMBERT-CLAUDE, Véronique
,
KASSIOTIS, Philippe
,
BURESI, Catherine
,
MALAFOSSE, Alain
,
JEANPIERRE, Marc
,
OUAZZANI, Réda
,
MRABET, Amel
,
MORRIS, Mike
,
LEGUEM, Eric
,
DRAVET, Charlotte
,
MAUGUIERE, Francois
Published in
Human genetics
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Molecular and Clinical Correlations in Autosomal Dominant Cerebellar Ataxia with Progressive Macular Dystrophy (SCA7)
by
David, Gilles
,
Dürr, Alexandra
,
Stevanin, Giovanni
,
Cancel, Géraldine
,
Abbas, Nacer
,
Benomar, Ali
,
Belal, Samir
,
Lebre, Anne-Sophie
,
Abada-Bendib, Myriem
,
Grid, Djamel
,
Holmberg, Monica
,
Yahyaoui, Mohamed
,
Hentati, Fayçal
,
Chkili, Taïeb
,
Agid, Yves
,
Brice, Alexis
Published in
Human molecular genetics
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A Locus for an Axonal Form of Autosomal Recessive Charcot-Marie-Tooth Disease Maps to Chromosome 1q21.2-q21.3
by
Bouhouche, Ahmed
,
Benomar, Ali
,
Birouk, Nazha
,
Mularoni, Angélique
,
Meggouh, Farid
,
Tassin, Johann
,
Grid, Djamal
,
Vandenberghe, Antoon
,
Yahyaoui, Mohamed
,
Chkili, Taïeb
,
Brice, Alexis
,
LeGuern, Eric
Published in
American journal of human genetics
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Vitamin E deficiency ataxia associated with adenoma
by
Benomar, Ali
,
Yahyaoui, Mohammed
,
Marzouki, Naima
,
Birouk, Nezha
,
Bouslam, Naima
,
Belaidi, Halima
,
Amarti, Afaf
,
Ouazzani, Reda
,
Chkili, Taieb
Published in
Journal of the neurological sciences
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The first de novo mutation of the connexin 32 gene associated with X linked Charcot-Marie-Tooth disease
by
Meggouh, F
,
Benomar, A
,
Rouger, H
,
Tardieu, S
,
Birouk, N
,
Tassin, J
,
Barhoumi, C
,
Yahyaoui, M
,
Chkili, T
,
Brice, A
,
LeGuern, E
Published in
Journal of medical genetics
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Mutations in MTMR13, a New Pseudophosphatase Homologue of MTMR2 and Sbf1, in Two Families with an Autosomal Recessive Demyelinating Form of Charcot-Marie-Tooth Disease Associated w...
by
Azzedine, H.
,
Bolino, A.
,
Taïeb, T.
,
Birouk, N.
,
Di Duca, M.
,
Bouhouche, A.
,
Benamou, S.
,
Mrabet, A.
,
Hammadouche, T.
,
Chkili, T.
,
Gouider, R.
,
Ravazzolo, R.
,
Brice, A.
,
Laporte, J.
,
LeGuern, E.
Published in
American journal of human genetics
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