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UnknownAssociation of a structural variant within the SQSTM1 gene with amyotrophic lateral sclerosis.
Not available
S-EPMC7061286 | biostudies-literature
UnknownDisease-modifying effects of an SCAF4 structural variant in a predominantly SOD1 ALS cohort.
Not available
S-EPMC7357414 | biostudies-literature
UnknownNovel STMN2 Variant Linked to Amyotrophic Lateral Sclerosis Risk and Clinical Phenotype.
Not available
S-EPMC8033025 | biostudies-literature
UnknownMutations in the nebulin gene associated with autosomal recessive nemaline myopathy.
Not available
S-EPMC26779 | biostudies-literature
UnknownClinical practice and effect of carbon dioxide on outcomes in mechanically ventilated acute brain-injured patients: a secondary analysis of the ENIO study.
Not available
S-EPMC10907416 | biostudies-literature
UnknownStandards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC).
Not available
S-EPMC9081216 | biostudies-literature
UnknownThe 5th edition of the World Health Organization Classification of Haematolymphoid Tumours: Myeloid and Histiocytic/Dendritic Neoplasms.
Not available
S-EPMC9252913 | biostudies-literature
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