Matches in Nanopublications for { ?s ?p "[Mucopolysaccharidosis type IIIA (MPSIIIA) is a lysosomal storage disorder caused by mutations in N-sulfoglucosamine sulfohydrolase (SGSH), resulting in heparan sulfate (HS) accumulation and progressive neurodegeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP692691.RA_2cqm6IGQNtYl4JU8t6T5-mICRKkK2AJQ2GAY0HP1ik130_assertion description "[Mucopolysaccharidosis type IIIA (MPSIIIA) is a lysosomal storage disorder caused by mutations in N-sulfoglucosamine sulfohydrolase (SGSH), resulting in heparan sulfate (HS) accumulation and progressive neurodegeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP692691.RA_2cqm6IGQNtYl4JU8t6T5-mICRKkK2AJQ2GAY0HP1ik130_provenance.
- NP1084343.RAYCecKf4P12TDAR2hJqDREaMUe96I3-DIIcc3ovr9UUk130_assertion description "[Mucopolysaccharidosis type IIIA (MPSIIIA) is a lysosomal storage disorder caused by mutations in N-sulfoglucosamine sulfohydrolase (SGSH), resulting in heparan sulfate (HS) accumulation and progressive neurodegeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1084343.RAYCecKf4P12TDAR2hJqDREaMUe96I3-DIIcc3ovr9UUk130_provenance.