Filamin B Loss-of-Function Mutation in Dimerization Domain Causes Autosomal-Recessive Spondylocarpotarsal Synostosis Syndrome with Rib Anomalies.
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Filamin B Loss-of-Function Mutation in Dimerization Domain Causes Autosomal-Recessive Spondylocarpotarsal Synostosis Syndrome with Rib Anomalies.
description
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name
Filamin B Loss-of-Function Mut ...... s Syndrome with Rib Anomalies.
@en
Filamin B Loss-of-Function Mut ...... s Syndrome with Rib Anomalies.
@nl
type
label
Filamin B Loss-of-Function Mut ...... s Syndrome with Rib Anomalies.
@en
Filamin B Loss-of-Function Mut ...... s Syndrome with Rib Anomalies.
@nl
prefLabel
Filamin B Loss-of-Function Mut ...... s Syndrome with Rib Anomalies.
@en
Filamin B Loss-of-Function Mut ...... s Syndrome with Rib Anomalies.
@nl
P2093
P2860
P356
P1433
P1476
Filamin B Loss-of-Function Mut ...... s Syndrome with Rib Anomalies.
@en
P2093
Chi-Fan Yang
Chun-Ping Chang
Chung-Hsing Wang
Fuu-Jen Tsai
Jer-Yuarn Wu
Wei-De Lin
Weng Siong H'ng
P2860
P304
P356
10.1002/HUMU.23186
P577
2017-02-01T00:00:00Z