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Cardiolipin Biosynthesis CL(i-12:0/i-20:0/a-25:0/a-25:0)
smpdb.ca/view/SMP0053741DiseaseA 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/i-22:0/a-25:0/a-25:0)
smpdb.ca/view/SMP0054389DiseaseA 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/i-24:0/a-25:0/a-25:0)
smpdb.ca/view/SMP0054709DiseaseA 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-17:0/a-25:0/a-25:0)
smpdb.ca/view/SMP0056005DiseaseA 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-13:0)
smpdb.ca/view/SMP0056650DiseaseA 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-12:0)
smpdb.ca/view/SMP0056655DiseaseA 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-14:0)
smpdb.ca/view/SMP0056657DiseaseA 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-17:0)
smpdb.ca/view/SMP0056660DiseaseA 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-18:0)
smpdb.ca/view/SMP0056663DiseaseA 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-21:0)
smpdb.ca/view/SMP0056666DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).