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Cardiolipin Biosynthesis CL(i-12:0/a-25:0/a-25:0/i-24:0)
smpdb.ca/view/SMP0050844DiseaseA 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-12:0/a-25:0)
smpdb.ca/view/SMP0050850DiseaseA 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-14:0/a-25:0)
smpdb.ca/view/SMP0050886DiseaseA 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-17:0/a-25:0)
smpdb.ca/view/SMP0050940DiseaseA 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-18:0/a-25:0)
smpdb.ca/view/SMP0050959DiseaseA 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-19:0/a-25:0)
smpdb.ca/view/SMP0050976DiseaseA 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-20:0/a-25:0)
smpdb.ca/view/SMP0050994DiseaseA 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-14:0/a-25:0/a-25:0)
smpdb.ca/view/SMP0051804DiseaseA 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-17:0/a-25:0/a-25:0)
smpdb.ca/view/SMP0052773DiseaseA 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-18:0/a-25:0/a-25:0)
smpdb.ca/view/SMP0053096DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).