Rare FOXC1 variants in congenital glaucoma: identification of translation regulatory sequences.
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Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development.Evaluating the association of bone morphogenetic protein 4-V152A and SIX homeobox 6-H141N polymorphisms with congenital cataract and microphthalmia in Western Indian population.
P2860
Rare FOXC1 variants in congenital glaucoma: identification of translation regulatory sequences.
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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 29 July 2015
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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
Rare FOXC1 variants in congeni ...... nslation regulatory sequences.
@en
Rare FOXC1 variants in congeni ...... nslation regulatory sequences.
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type
label
Rare FOXC1 variants in congeni ...... nslation regulatory sequences.
@en
Rare FOXC1 variants in congeni ...... nslation regulatory sequences.
@nl
prefLabel
Rare FOXC1 variants in congeni ...... nslation regulatory sequences.
@en
Rare FOXC1 variants in congeni ...... nslation regulatory sequences.
@nl
P2093
P2860
P50
P356
P1476
Rare FOXC1 variants in congeni ...... nslation regulatory sequences.
@en
P2093
Cristina Medina-Trillo
Laura Morales
Maite García-Antón
P2860
P2888
P304
P356
10.1038/EJHG.2015.169
P577
2015-07-29T00:00:00Z