Title : An Indian family with Sjögren-Larsson syndrome caused by a novel ALDH3A2 mutation.

Pub. Date : 2010 Sep

PMID : 20883264






4 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 The aspartic acid residue at the mutation site is located in the C-terminal portion of the second a-helix strand, a2, of N-terminal four helices of FALDH and the FALDH amino-acid sequence alignment shows that this aspartic acid residue is conserved among several diverse species. Aspartic Acid aldehyde dehydrogenase 3 family member A2 Homo sapiens
2 The aspartic acid residue at the mutation site is located in the C-terminal portion of the second a-helix strand, a2, of N-terminal four helices of FALDH and the FALDH amino-acid sequence alignment shows that this aspartic acid residue is conserved among several diverse species. Aspartic Acid aldehyde dehydrogenase 3 family member A2 Homo sapiens
3 The aspartic acid residue at the mutation site is located in the C-terminal portion of the second a-helix strand, a2, of N-terminal four helices of FALDH and the FALDH amino-acid sequence alignment shows that this aspartic acid residue is conserved among several diverse species. Aspartic Acid aldehyde dehydrogenase 3 family member A2 Homo sapiens
4 The aspartic acid residue at the mutation site is located in the C-terminal portion of the second a-helix strand, a2, of N-terminal four helices of FALDH and the FALDH amino-acid sequence alignment shows that this aspartic acid residue is conserved among several diverse species. Aspartic Acid aldehyde dehydrogenase 3 family member A2 Homo sapiens