Novel and recurrent PITX3 mutations in Belgian families with autosomal dominant congenital cataract and anterior segment dysgenesis have similar phenotypic and functional characteristics.
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Prostaglandins in the eye: Function, expression, and roles in glaucoma.A novel nonsense mutation in the MIP gene linked to congenital posterior polar cataracts in a Chinese family.Interocular anatomical and visual functional differences in pediatric patients with unilateral cataractsMutation update of transcription factor genes FOXE3, HSF4, MAF, and PITX3 causing cataracts and other developmental ocular defects.A child with Myhre syndrome presenting with corectopia and tetralogy of Fallot.Molecular Genetics of Cataract.
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Novel and recurrent PITX3 mutations in Belgian families with autosomal dominant congenital cataract and anterior segment dysgenesis have similar phenotypic and functional characteristics.
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article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 20 February 2014
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Novel and recurrent PITX3 muta ...... nd functional characteristics.
@en
Novel and recurrent PITX3 muta ...... nd functional characteristics.
@nl
type
label
Novel and recurrent PITX3 muta ...... nd functional characteristics.
@en
Novel and recurrent PITX3 muta ...... nd functional characteristics.
@nl
prefLabel
Novel and recurrent PITX3 muta ...... nd functional characteristics.
@en
Novel and recurrent PITX3 muta ...... nd functional characteristics.
@nl
P2093
P2860
P356
P1476
Novel and recurrent PITX3 muta ...... nd functional characteristics.
@en
P2093
Elena A Sorokina
Elfride De Baere
Françoise Meire
Hannah Verdin
Ingele Casteels
Thomy de Ravel
P2860
P2888
P356
10.1186/1750-1172-9-26
P577
2014-02-20T00:00:00Z
P5875
P6179
1006951640