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HUMU.23186
HUMU.23186
http://dx.doi.org/10.1002/HUMU.23186
Filamin B Loss-of-Function Mutation in Dimerization Domain Causes Autosomal-Recessive Spondylocarpotarsal Synostosis Syndrome with Rib Anomalies.
P356
Q51158820-67E11446-B665-4BC2-8813-1E7DC5B105DE
P356
HUMU.23186
http://dx.doi.org/10.1002/HUMU.23186