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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).
Cardiolipin Biosynthesis CL(i-13:0/a-13:0/a-25:0/a-25:0)
smpdb.ca/view/SMP0055358DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).
Cardiolipin Biosynthesis CL(i-13:0/a-15:0/a-25:0/a-25:0)
smpdb.ca/view/SMP0055681DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).
Cardiolipin Biosynthesis CL(i-13:0/a-21:0/a-25:0/a-25:0)
smpdb.ca/view/SMP0056329DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).
Cardiolipin Biosynthesis CL(i-13:0/a-25:0/a-13:0/a-25:0)
smpdb.ca/view/SMP0056583DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).
Cardiolipin Biosynthesis CL(i-13:0/a-25:0/a-15:0/a-25:0)
smpdb.ca/view/SMP0056601DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).
Cardiolipin Biosynthesis CL(i-13:0/a-25:0/a-17:0/a-25:0)
smpdb.ca/view/SMP0056619DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).
Cardiolipin Biosynthesis CL(i-13:0/a-25:0/a-25:0/a-15:0)
smpdb.ca/view/SMP0056651DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).
Cardiolipin Biosynthesis CL(i-13:0/a-25:0/a-25:0/i-13:0)
smpdb.ca/view/SMP0056656DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).
Cardiolipin Biosynthesis CL(i-13:0/a-25:0/a-25:0/i-16:0)
smpdb.ca/view/SMP0056659DiseaseA mutated tafazzin gene disrupts this post-synthetic remodeling and causes Barth syndrome (BTHS), an X-linked human disease (PMID: 16973164).