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Cardiolipin Biosynthesis CL(i-12:0/i-12:0/a-25:0/a-25:0)
smpdb.ca/view/SMP0051157DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).
Cardiolipin Biosynthesis CL(i-13:0/a-25:0/a-21:0/a-25:0)
smpdb.ca/view/SMP0056636DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).
Cardiolipin Biosynthesis CL(i-13:0/a-25:0/a-25:0/a-17:0)
smpdb.ca/view/SMP0056652DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).
Cardiolipin Biosynthesis CL(i-13:0/a-25:0/a-25:0/a-21:0)
smpdb.ca/view/SMP0056653DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).
Cardiolipin Biosynthesis CL(i-13:0/a-25:0/a-25:0/i-15:0)
smpdb.ca/view/SMP0056658DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).
Cardiolipin Biosynthesis CL(i-13:0/a-25:0/a-25:0/i-22:0)
smpdb.ca/view/SMP0056667DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).
Cardiolipin Biosynthesis CL(i-13:0/a-25:0/i-13:0/a-25:0)
smpdb.ca/view/SMP0056692DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).
Cardiolipin Biosynthesis CL(i-13:0/a-25:0/i-15:0/a-25:0)
smpdb.ca/view/SMP0056728DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).
Cardiolipin Biosynthesis CL(i-13:0/a-25:0/i-16:0/a-25:0)
smpdb.ca/view/SMP0056746DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).
Cardiolipin Biosynthesis CL(i-13:0/a-25:0/i-17:0/a-25:0)
smpdb.ca/view/SMP0056764DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).