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Cardiolipin Biosynthesis CL(i-13:0/a-25:0/a-25:0/i-20:0)
smpdb.ca/view/SMP0056665DiseaseA 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-24:0)
smpdb.ca/view/SMP0056668DiseaseA 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-12:0/a-25:0)
smpdb.ca/view/SMP0056674DiseaseA 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/i-14:0/a-25:0/a-25:0)
smpdb.ca/view/SMP0057635DiseaseA 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/i-16:0/a-25:0/a-25:0)
smpdb.ca/view/SMP0058282DiseaseA 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/i-18:0/a-25:0/a-25:0)
smpdb.ca/view/SMP0058941DiseaseA 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/i-20:0/a-25:0/a-25:0)
smpdb.ca/view/SMP0059598DiseaseA 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/i-22:0/a-25:0/a-25:0)
smpdb.ca/view/SMP0060275DiseaseA 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/i-24:0/a-25:0/a-25:0)
smpdb.ca/view/SMP0060597DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).
Cardiolipin Biosynthesis CL(i-14:0/a-13:0/a-25:0/a-25:0)
smpdb.ca/view/SMP0060925DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).