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Accession: PRJNA839144 ID: 839144

Homo sapiens (human)

Homo sapiens Raw sequence reads

See Genome Information for Homo sapiens
Two patients with SMA-LED caused by DYNC1H1 mutations were reported, with an aim to explore the phenotypic and genetic spectrum of neuromuscular diseases caused by DYNC1H1 mutations by systematically reviewing previous relevant publications. The genotype-phenotype correlations of this gene mutation was further analyzed.
AccessionPRJNA839144
Data TypeRaw sequence reads
ScopeMultiisolate
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
SubmissionRegistration date: 17-May-2022
Huashan Hospital, Fudan University
Project Data:
No public data is linked to this project. Any recently released data that cites this project will be linked to it within a few days.

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