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Cardiolipin Biosynthesis CL(a-13:0/a-25:0/a-25:0/i-12:0)
smpdb.ca/view/SMP0045030DiseaseA 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/a-25:0/i-14:0)
smpdb.ca/view/SMP0045032DiseaseA 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-14:0/a-25:0)
smpdb.ca/view/SMP0045083DiseaseA 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-16:0/a-25:0)
smpdb.ca/view/SMP0045119DiseaseA 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-19:0/a-25:0)
smpdb.ca/view/SMP0045173DiseaseA 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-20:0/a-25:0)
smpdb.ca/view/SMP0045191DiseaseA 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-13:0/a-25:0/a-25:0)
smpdb.ca/view/SMP0045672DiseaseA 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-16:0/a-25:0/a-25:0)
smpdb.ca/view/SMP0046639DiseaseA 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-17:0/a-25:0/a-25:0)
smpdb.ca/view/SMP0046963DiseaseA 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-19:0/a-25:0/a-25:0)
smpdb.ca/view/SMP0047608DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).