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A mutation in PNPT1, encoding mitochondrial-RNA-import protein PNPase, causes hereditary hearing loss.
24 auth.
Simon von Ameln,
Geng Wang,
Redouane Boulouiz,
M. Rutherford,
Geoffrey M. Smith,
Yun Li,
Hans-Martin Pogoda,
G. Nürnberg,
Barbara Stiller,
A. Volk,
...
G. Borck,
Jason S. Hong,
R. Goodyear,
O. Abidi,
P. Nürnberg,
K. Hofmann,
G. Richardson,
M. Hammerschmidt,
T. Moser,
B. Wollnik,
C. Koehler,
M. Teitell,
A. Barakat,
C. Kubisch
|
6 |
2012 |
6
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|
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Mutations in TPRN cause a progressive form of autosomal-recessive nonsyndromic hearing loss.
16 auth.
Yun Li,
E. Pohl,
Redouane Boulouiz,
M. Schraders,
G. Nürnberg,
M. Charif,
R. Admiraal,
Simon von Ameln,
Ingelore Baessmann,
M. Kandil,
...
J. Veltman,
P. Nürnberg,
C. Kubisch,
A. Barakat,
H. Kremer,
B. Wollnik
|
5 |
2010 |
5
🐜
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|
🐜
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AZF microdeletions and partial deletions of AZFc region on the Y chromosome in Moroccan men.
13 auth.
Laila Imken,
B. El houate,
A. Chafik,
Halima Nahili,
Redouane Boulouiz,
O. Abidi,
Elbakkay Chadli,
N. Louanjli,
Abdelouhab Elfath,
M. Hassar,
...
K. McElreavey,
A. Barakat,
H. Rouba
|
5 |
2007 |
5
🐜
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|
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GJB2 (connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2-35delG mutation.
11 auth.
O. Abidi,
Redouane Boulouiz,
Halima Nahili,
Mohammed Ridal,
M. Alami,
A. Tlili,
...
H. Rouba,
S. Masmoudi,
A. Chafik,
M. Hassar,
A. Barakat
|
5 |
2007 |
5
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|
|
🐬
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Distribution and features of hematological malignancies in Eastern Morocco: a retrospective multicenter study over 5 years
Mounia Elidrissi Errahhali,
Manal Elidrissi Errahhali,
Redouane Boulouiz,
M. Ouarzane,
M. Bellaoui
|
5 |
2016 |
5
🐬
|
|
🐜
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Association Analysis of IGF2BP2, KCNJ11, and CDKAL1 Polymorphisms with Type 2 Diabetes Mellitus in a Moroccan Population: A Case–Control Study and Meta-analysis
9 auth.
H. Benrahma,
H. Charoute,
Khaled Lasram,
Redouane Boulouiz,
R. Atig,
M. Fakiri,
...
H. Rouba,
S. Abdelhak,
A. Barakat
|
5 |
2014 |
5
🐜
|
|
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Recessive TBC1D24 Mutations Are Frequent in Moroccan Non-Syndromic Hearing Loss Pedigrees
8 auth.
Amina Bakhchane,
M. Charif,
Sara Salime,
Redouane Boulouiz,
Halima Nahili,
R. Roky,
...
G. Lenaers,
A. Barakat
|
4 |
2015 |
4
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|
|
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No Association between T222P/LGR8 Mutation and Cryptorchidism in the Moroccan Population
10 auth.
B. El houate,
H. Rouba,
Laila Imken,
Hicham Sibai,
A. Chafik,
Redouane Boulouiz,
...
Elbakkay Chadli,
Mohmmed Hassar,
K. McElreavey,
A. Barakat
|
4 |
2008 |
4
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