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Human Genomics, ISSN 1473-9542, 2011, Volume 5, Issue 3, pp. 156 - 169
Lysosomal storage disorders (LSDs) are a large group of more than 50 different inherited metabolic diseases which, in the great majority of cases, result from... 
Lysosomal Storage Diseases - diagnosis | Specimen Handling | Phenotype | Proteins - metabolism | Humans | Chorionic Villi Sampling | Lysosomal Storage Diseases - genetics | Lysosomal Storage Diseases - metabolism | Genotype | Prenatal Diagnosis - methods | Genetic Testing - methods | Polymorphism, Genetic
Journal Article
Molecular Phylogenetics and Evolution, ISSN 1055-7903, 03/2012, Volume 62, Issue 3, pp. 889 - 897
► The genus (Orchidaceae) was not monophyletic. None of the sections of were monophyletic. ► Monophyly of subtribe Chloraeinae was corroborated. ► Neither nor... 
Molecular phylogeny | South American orchids | rpoC1 | nrITS | Chloraeinae | matK-trnK | Gavilea | atpB-rbcL | AtpB-rbcL | NrITS | RpoC1 | MatK-trnK | NRDNA | BIOCHEMISTRY & MOLECULAR BIOLOGY | SUPPORT | EVOLUTIONARY BIOLOGY | GENETICS & HEREDITY | DNA-SEQUENCE DATA | PROGRAM | Orchidaceae - genetics | Plastids - genetics | DNA, Ribosomal Spacer - chemistry | Phylogeny | Orchidaceae - classification
Journal Article
Metabolic Brain Disease, ISSN 0885-7490, 10/2017, Volume 32, Issue 5, pp. 1529 - 1536
Journal Article
ChemBioChem, ISSN 1439-4227, 09/2015, Volume 16, Issue 14, p. 2054
A collection of carbohydrate-derived iminosugars belonging to three structurally diversified sub-classes (polyhydroxylated pyrrolidines, piperidines, and... 
Enzymes | Hydrolases
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