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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).
Cardiolipin Biosynthesis CL(i-12:0/a-25:0/a-13:0/a-25:0)
smpdb.ca/view/SMP0050760DiseaseA 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-20:0)
smpdb.ca/view/SMP0050841DiseaseA 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-22:0)
smpdb.ca/view/SMP0050843DiseaseA 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/i-24:0/a-25:0)
smpdb.ca/view/SMP0051049DiseaseA 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-13:0/a-25:0/a-25:0)
smpdb.ca/view/SMP0051481DiseaseA 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-15:0/a-25:0/a-25:0)
smpdb.ca/view/SMP0052127DiseaseA 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-16:0/a-25:0/a-25:0)
smpdb.ca/view/SMP0052450DiseaseA 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-19:0/a-25:0/a-25:0)
smpdb.ca/view/SMP0053419DiseaseA 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-21:0/a-25:0/a-25:0)
smpdb.ca/view/SMP0054066DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).