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Journal articles
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A novel mutation of PARK-2 gene in a patient with early-onset Parkinson's disease.
Alafifi, Tariq.
Oman Medical Specialty Board.
2020-05
A novel mutation of PARK-2 gene in a patient with early-onset Parkinson's disease.
Journal articles
0
0
Sanjad-Sakati Syndrome in Omani children.
Rafique, Bushra.
Oman Medical Specialty Board.
2010-07
Sanjad-Sakati Syndrome in Omani children.
Theses and Dissertations
0
0
Genomic studies of autosomal recessive epilepsies in three Omani consanguineous families
Basak, Saroma.
Sultan Qaboos University
2016
Genomic studies of autosomal recessive epilepsies in three Omani consanguineous families
Journal articles
0
0
Mutation in the PCSK9 gene in Omani Arab subjects with autosomal dominant hypercholesterolemia and its effect on PCSK9 protein structure.
Al-Waili, Khalid.
Oman Medical Specialty Board.
2013-01
Mutation in the PCSK9 gene in Omani Arab subjects with autosomal dominant hypercholesterolemia and its effect on PCSK9 protein structure.
Journal articles
0
0
Autosomal dominant polycystic kidney disease and pericardial effusion.
Fernandez, Guillermo Alberto Perez.
Oman Medical Specialty Board.
2018-09
Autosomal dominant polycystic kidney disease and pericardial effusion.
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English
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Journal articles
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Theses and Dissertations
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Journal articles
(4)
Theses and Dissertations
(1)
Subject
Autosomal dominant hypercholesterolemia
(1)
Autosomal recessive disorder
(1)
Autosomal recessive epilepsies
(1)
Autosomal recessive Parkinsonism
(1)
biochemistry
(1)
Chronic renal diseases
(1)
Codon, Nonsense
(1)
Codon, Terminator
(1)
Genomics
(1)
Molecular biology
(1)
Mutation
(1)
Omani consanguineous families
(1)
PARK 2 protein, Human
(1)
Parkinson's disease
(1)
PCSK9 protien
(1)
Pericardial effusion
(1)
Polycystic kidney, Autosomal dominant
(1)
Sanjad Sakati syndrome
(1)
Author
Al-Waili, Khalid.
(1)
Alafifi, Tariq.
(1)
Basak, Saroma.
(1)
Fernandez, Guillermo Alberto Perez.
(1)
Rafique, Bushra.
(1)
Publisher
Oman Medical Specialty Board
(4)
Sultan Qaboos University
(1)
sfy39587stp18
