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Search Results - Shinwari, Zarghuna Ma
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A substitution mutation in cardiac ubiquitin ligase, FBXO32, is associated with an autosomal recessive form of dilated cardiomyopathy
by
Al-Hassnan, Zuhair N
,
Shinwari, Zarghuna Ma
,
Wakil, Salma M
,
Tulbah, Sahar
,
Mohammed, Shamayel
,
Rahbeeni, Zuhair
,
Alghamdi, Mohammed
,
Rababh, Monther
,
Colak, Dilek
,
Kaya, Namik
,
Al-Fayyadh, Majid
,
Alburaiki, Jehad
Published in
BMC medical genetics
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Bmc Medical Genetics
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Adolescent
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Amino Acid Sequence
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Analysis
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Blood Pressure
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Cardiomyopathy
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Cardiomyopathy, Dilated
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Cardiomyopathy, Dilated - Genetics
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Chromosome Mapping
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Chromosomes
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Computational Biology
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Deoxyribonucleic Acid
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Dna
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Edema
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Fbxo32
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