Hasil Pencarian (1)
biotech | CAS: 1480724-61-5
Achondroplasia is an autosomal dominant genetic disease and the most common cause of dwarfism in humans.[A242277] It results from a gain-of-function missense mutation in _FGFR3_ that results in a dramatic suppression of bone growth, both in volume and in leng…
Kategori:
Amino Acids, Peptides, and ProteinsC-type Natriuretic Peptide AnalogDrugs Affecting Bone Structure and Mineralization
+7
Target Protein:
Atrial natriuretic peptide receptor 2
Waktu ParuhThe mean half-life …
Vol. DistribusiThe mean apparent v…
KlirensThe mean apparent c…
Genetik
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