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Cardiolipin Biosynthesis CL(a-13:0/a-25:0/i-13:0/a-25:0)
smpdb.ca/view/SMP0045065DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).
Cardiolipin Biosynthesis CL(a-13:0/a-25:0/i-17:0/a-25:0)
smpdb.ca/view/SMP0045137DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).
Cardiolipin Biosynthesis CL(a-13:0/a-25:0/i-21:0/a-25:0)
smpdb.ca/view/SMP0045209DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).
Cardiolipin Biosynthesis CL(a-13:0/a-25:0/i-24:0/a-25:0)
smpdb.ca/view/SMP0045245DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).
Cardiolipin Biosynthesis CL(a-13:0/i-14:0/a-25:0/a-25:0)
smpdb.ca/view/SMP0045993DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).
Cardiolipin Biosynthesis CL(a-13:0/i-15:0/a-25:0/a-25:0)
smpdb.ca/view/SMP0046317DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).
Cardiolipin Biosynthesis CL(a-13:0/i-18:0/a-25:0/a-25:0)
smpdb.ca/view/SMP0047286DiseaseA 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-13:0/a-25:0/a-25:0)
smpdb.ca/view/SMP0049541DiseaseA 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-15:0/a-25:0/a-25:0)
smpdb.ca/view/SMP0049862DiseaseA 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-21:0/a-25:0/a-25:0)
smpdb.ca/view/SMP0050508DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).