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- NP81234.RARjozuSXTjn8igrKjzEJ0SNTkG5oS9yCqZF7v6JLY1M0130_assertion description "[In SPTLC1, we detected a novel mutation (S331F) corresponding to a previously unknown severe and early-onset HSAN phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81234.RARjozuSXTjn8igrKjzEJ0SNTkG5oS9yCqZF7v6JLY1M0130_provenance.
- assertion description "[In SPTLC1, we detected a novel mutation (S331F) corresponding to a previously unknown severe and early-onset HSAN phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[In SPTLC1, we detected a novel mutation (S331F) corresponding to a previously unknown severe and early-onset HSAN phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP755126.RAd2AybXhaLL1CgXeAZoUdimvMyQ5sSyhpU2fFlvBfcR8130_assertion description "[In SPTLC1, we detected a novel mutation (S331F) corresponding to a previously unknown severe and early-onset HSAN phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP755126.RAd2AybXhaLL1CgXeAZoUdimvMyQ5sSyhpU2fFlvBfcR8130_provenance.
- NP847075.RAre3mzPGLtIqMXLZleBpdMf8iyget56jvWltZmXg5HJg130_assertion description "[In SPTLC1, we detected a novel mutation (S331F) corresponding to a previously unknown severe and early-onset HSAN phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP847075.RAre3mzPGLtIqMXLZleBpdMf8iyget56jvWltZmXg5HJg130_provenance.
- NP153873.RAtNRfF2n8kRDTlOaXMBvEoo7_B6o48FQEWpquMfVgVm8130_assertion description "[In SPTLC1, we detected a novel mutation (S331F) corresponding to a previously unknown severe and early-onset HSAN phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP153873.RAtNRfF2n8kRDTlOaXMBvEoo7_B6o48FQEWpquMfVgVm8130_provenance.
- NP123851.RAOERZtY0xeHrWnz3NpIGm1NJYfEKoXGCfFq3DmxHI--s130_assertion description "[In SPTLC1, we detected a novel mutation (S331F) corresponding to a previously unknown severe and early-onset HSAN phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP123851.RAOERZtY0xeHrWnz3NpIGm1NJYfEKoXGCfFq3DmxHI--s130_provenance.