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neuropilin-1 isoform c precursor [Homo sapiens]
neuropilin-1 isoform c precursor [Homo sapiens]
gi|1844084081|ref|NP_001019800.2|
Protein
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Werner Syndrome
Werner Syndrome
An autosomal recessive disorder that causes premature aging in adults, characterized by sclerodermal skin changes, cataracts, subcutaneous calcification, muscular atrophy, a t...<br/>Year introduced: 1998
MeSH
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