Mutations in KIF21A and PHOX2A are absent in 16 patients with congenital vertical incomitant strabismus.
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Lack of KIF21A mutations in congenital fibrosis of the extraocular muscles type I patients from consanguineous Saudi Arabian families.Retinal Dysfunction in Patients with Congenital Fibrosis of the Extraocular Muscles Type 2.Recessive mutations in COL25A1 are a cause of congenital cranial dysinnervation disorderMiR-326 regulates cell proliferation and migration in lung cancer by targeting phox2a and is regulated by HOTAIR.The optic nerve head in congenital fibrosis of the extraocular muscles.
P2860
Mutations in KIF21A and PHOX2A are absent in 16 patients with congenital vertical incomitant strabismus.
description
2009 nî lūn-bûn
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2009年の論文
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2009年学术文章
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2009年学术文章
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2009年学术文章
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2009年学术文章
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name
Mutations in KIF21A and PHOX2A ...... ertical incomitant strabismus.
@en
Mutations in KIF21A and PHOX2A ...... ertical incomitant strabismus.
@nl
type
label
Mutations in KIF21A and PHOX2A ...... ertical incomitant strabismus.
@en
Mutations in KIF21A and PHOX2A ...... ertical incomitant strabismus.
@nl
prefLabel
Mutations in KIF21A and PHOX2A ...... ertical incomitant strabismus.
@en
Mutations in KIF21A and PHOX2A ...... ertical incomitant strabismus.
@nl
P2093
P2860
P1433
P1476
Mutations in KIF21A and PHOX2A ...... vertical incomitant strabismus
@en
P2093
Arif O Khan
Dania S Khalil
Latifa J Al-Sharif
P2860
P304
P356
10.3109/13816810903183613
P577
2009-12-01T00:00:00Z