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Cardiolipin Biosynthesis CL(a-13:0/i-22:0/a-25:0/a-25:0)
smpdb.ca/view/SMP0048572DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).
Cardiolipin Biosynthesis CL(i-12:0/a-17:0/a-25:0/a-25:0)
smpdb.ca/view/SMP0050186DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).
Cardiolipin Biosynthesis CL(i-12:0/a-25:0/a-15:0/a-25:0)
smpdb.ca/view/SMP0050778DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).
Cardiolipin Biosynthesis CL(i-12:0/a-25:0/a-17:0/a-25:0)
smpdb.ca/view/SMP0050796DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).
Cardiolipin Biosynthesis CL(i-12:0/a-25:0/a-21:0/a-25:0)
smpdb.ca/view/SMP0050814DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).
Cardiolipin Biosynthesis CL(i-12:0/a-25:0/a-25:0/a-15:0)
smpdb.ca/view/SMP0050829DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).
Cardiolipin Biosynthesis CL(i-12:0/a-25:0/a-25:0/a-17:0)
smpdb.ca/view/SMP0050830DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).
Cardiolipin Biosynthesis CL(i-12:0/a-25:0/a-25:0/i-14:0)
smpdb.ca/view/SMP0050835DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).
Cardiolipin Biosynthesis CL(i-12:0/a-25:0/a-25:0/i-18:0)
smpdb.ca/view/SMP0050839DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).
Cardiolipin Biosynthesis CL(i-12:0/a-25:0/a-25:0/i-19:0)
smpdb.ca/view/SMP0050840DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).