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TOR1A variants cause a severe arthrogryposis with developmental delay, strabismus and tremor
by
Kariminejad, Ariana
,
Dahl-Halvarsson, Martin
,
Ravenscroft, Gianina
,
Afroozan, Fariba
,
Keshavarz, Elham
,
Goullée, Hayley
,
Davis, Mark R
,
Faraji Zonooz, Mehrshid
,
Najmabadi, Hossein
,
Laing, Nigel G
,
Tajsharghi, Homa
Published in
Brain (London, England : 1878)
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P.493 - TOR1A variants cause a severe arthrogryposis with developmental delay, strabismus and tremor
by
Kariminejad, A.
,
Dahl-Halvarsson, M.
,
Ravenscroft, G.
,
Afroozan, F.
,
Keshavarz, E.
,
Goullée, H.
,
Davis, M.
,
Laing, N.
,
Tajsharghi, H.
Published in
Neuromuscular disorders : NMD
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TOR1A variants cause a severe arthrogryposis with developmental delay, strabismus and tremor
by
Kariminejad, A.
,
Dahl-Halvarsson, M.
,
Ravenscroft, G.
,
Afroozan, F.
,
Keshavarz, E.
,
Goullée, H.
,
Davis, M.
,
Laing, N.
,
Tajsharghi, H.
Published in
Neuromuscular disorders : NMD
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Elucidating the spectrum of {alpha}-thalassemia mutations in Iran
by
Hadavi, Valeh
,
Taromchi, Amir Hossein
,
Malekpour, Mahdi
,
Gholami, Behjat
,
Law, Hai-Yang
,
Almadani, Navid
,
Afroozan, Fariba
,
Sahebjam, Farhad
,
Pajouh, Parisa
,
Kariminejad, Roxana
,
Kariminejad, Mohammad Hassan
,
Azarkeivan, Azita
,
Jafroodi, Maryam
,
Tamaddoni, Ahmad
,
Puehringer, Helene
,
Oberkanins, Christian
,
Najmabadi, Hossein
Published in
Haematologica (Roma)
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Neuromuscular Disorders : Nmd
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Ashkenazi Jews
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