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Cardiolipin Biosynthesis CL(a-13:0/a-25:0/i-18:0/a-25:0)
smpdb.ca/view/SMP0045155DiseaseA 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-22:0/a-25:0)
smpdb.ca/view/SMP0045227DiseaseA 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-12:0/a-25:0/a-25:0)
smpdb.ca/view/SMP0045351DiseaseA 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-20:0/a-25:0/a-25:0)
smpdb.ca/view/SMP0047931DiseaseA 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-21:0/a-25:0/a-25:0)
smpdb.ca/view/SMP0048250DiseaseA 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-24:0/a-25:0/a-25:0)
smpdb.ca/view/SMP0048894DiseaseA 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/a-13:0)
smpdb.ca/view/SMP0050828DiseaseA 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/a-21:0)
smpdb.ca/view/SMP0050831DiseaseA 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-12:0)
smpdb.ca/view/SMP0050833DiseaseA 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-13:0)
smpdb.ca/view/SMP0050834DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).