A truncating mutation in GPSM2 is associated with recessive non-syndromic hearing loss.
about
Autosomal recessive nonsyndromic deafness genes: a reviewActivators of G protein signaling exhibit broad functionality and define a distinct core signaling triadLis1 mediates planar polarity of auditory hair cells through regulation of microtubule organization.Defective Gpsm2/Gαi3 signalling disrupts stereocilia development and growth cone actin dynamics in Chudley-McCullough syndromeGPSM2 mutations cause the brain malformations and hearing loss in Chudley-McCullough syndromeGroup II activators of G-protein signalling and proteins containing a G-protein regulatory motif.The Spindle Orientation Machinery Beyond Mitosis: When Cell Specialization Demands Polarization.The GPSM2/LGN GoLoco motifs are essential for hearing.GPSM2 mutations in Chudley-McCullough syndrome.
P2860
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P2860
A truncating mutation in GPSM2 is associated with recessive non-syndromic hearing loss.
description
2011 nî lūn-bûn
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2011年の論文
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2011年論文
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2011年論文
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2011年論文
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2011年論文
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2011年論文
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2011年论文
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2011年论文
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2011年论文
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name
A truncating mutation in GPSM2 is associated with recessive non-syndromic hearing loss.
@en
type
label
A truncating mutation in GPSM2 is associated with recessive non-syndromic hearing loss.
@en
prefLabel
A truncating mutation in GPSM2 is associated with recessive non-syndromic hearing loss.
@en
P2093
P2860
P1433
P1476
A truncating mutation in GPSM2 is associated with recessive non-syndromic hearing loss.
@en
P2093
P2860
P304
P356
10.1111/J.1399-0004.2011.01654.X
P577
2011-03-15T00:00:00Z