A postnatal role for embryonic myosin revealed by MYH3 mutations that alter TGFβ signaling and cause autosomal dominant spondylocarpotarsal synostosis.
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A novel pathogenic MYH3 mutation in a child with Sheldon-Hall syndrome and vertebral fusions.Recessive Spondylocarpotarsal Synostosis Syndrome Due to Compound Heterozygosity for Variants in MYH3Asymmetric expression of H19 and ADIPOQ in concave/convex paravertebral muscles is associated with severe adolescent idiopathic scoliosis
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A postnatal role for embryonic myosin revealed by MYH3 mutations that alter TGFβ signaling and cause autosomal dominant spondylocarpotarsal synostosis.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 16 February 2017
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
A postnatal role for embryonic ...... pondylocarpotarsal synostosis.
@en
A postnatal role for embryonic ...... pondylocarpotarsal synostosis.
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type
label
A postnatal role for embryonic ...... pondylocarpotarsal synostosis.
@en
A postnatal role for embryonic ...... pondylocarpotarsal synostosis.
@nl
prefLabel
A postnatal role for embryonic ...... pondylocarpotarsal synostosis.
@en
A postnatal role for embryonic ...... pondylocarpotarsal synostosis.
@nl
P2093
P2860
P356
P1433
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A postnatal role for embryonic ...... pondylocarpotarsal synostosis.
@en
P2093
Daniel H Cohn
Deborah Krakow
Deborah Nickerson
Dorothy K Grange
Jennifer Zieba
Jorge H Martin
Kelly Heard
Kimberly N Forlenza
Merlin G Butler
Michael Bamshad
P2860
P2888
P356
10.1038/SREP41803
P407
P577
2017-02-16T00:00:00Z