Search
Cardiolipin Biosynthesis CL(a-13:0/a-25:0/a-13:0/a-25:0)
smpdb.ca/view/SMP0044957DiseaseA 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-15:0/a-25:0)
smpdb.ca/view/SMP0044975DiseaseA 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/a-15:0)
smpdb.ca/view/SMP0045026DiseaseA 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/a-21:0)
smpdb.ca/view/SMP0045028DiseaseA 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-13:0)
smpdb.ca/view/SMP0045031DiseaseA 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-15:0)
smpdb.ca/view/SMP0045033DiseaseA 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-16:0)
smpdb.ca/view/SMP0045034DiseaseA 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-18:0)
smpdb.ca/view/SMP0045036DiseaseA 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-21:0)
smpdb.ca/view/SMP0045039DiseaseA 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-22:0)
smpdb.ca/view/SMP0045040DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).