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Search Results - Al‐Habsi, Asila
Search Results - Al‐Habsi, Asila
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A founder mutation in CA5A causing intrafamilial and interfamilial phenotypic variability in a cohort of 18 patients with carbonic anhydrase VA deficiency
by
Al‐Thihli, Khalid
,
Al Hashmi, Nadia
,
Al Balushi, Aaisha
,
Al‐Habsi, Asila
,
Al‐Ajmi, Eiman
,
Al‐Jasmi, Fatma
,
Al‐Murshedi, Fathiya
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JIMD reports
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CNP deficiency causes severe hypomyelinating leukodystrophy in humans
by
Al-Abdi, Lama
,
Al Murshedi, Fathiya
,
Elmanzalawy, Alaa
,
Al Habsi, Asila
,
Helaby, Rana
,
Ganesh, Anuradha
,
Ibrahim, Niema
,
Patel, Nisha
,
Alkuraya, Fowzan S.
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Human genetics
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Hypoketotic hypoglycemia without neuromuscular complications in patients with SLC25A32 deficiency
by
Al Shamsi, Bushra
,
Al Murshedi, Fathiya
,
Al Habsi, Asila
,
Al-Thihli, Khalid
Published in
European journal of human genetics : EJHG
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Biallelic variants in the synaptic vesicle glycoprotein 2 A are associated with epileptic encephalopathy
by
Al-Maawali, Almundher
,
Al-Murshedi, Fathiya
,
Al-Futaisi, Amna
,
Mansy, Ahmed
,
Al-Habsi, Asila
,
Girisha, Katta M
Published in
European journal of human genetics : EJHG
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Isolation, structure characterization and prediction of antioxidant activity of two new compounds from the leaves of Dodonaea viscosa native to the Sultanate of Oman
by
Al Habsi, Asila Ahmed Salim
,
Hossain, Mohammad Amzad
Published in
Egyptian Journal of Basic and Applied Sciences
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