Novel ABCA4 compound heterozygous mutations cause severe progressive autosomal recessive cone-rod dystrophy presenting as Stargardt disease.
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Dawn of ocular gene therapy: implications for molecular diagnosis in retinal diseaseABCA4 gene screening by next-generation sequencing in a British cohortNovel compound heterozygous mutations in ABCA4 in a Chinese pedigree with Stargardt disease.Generalized choriocapillaris dystrophy, a distinct phenotype in the spectrum of ABCA4-associated retinopathies.Identification of Novel Mutations in ABCA4 Gene: Clinical and Genetic Analysis of Indian Patients with Stargardt Disease.
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Novel ABCA4 compound heterozygous mutations cause severe progressive autosomal recessive cone-rod dystrophy presenting as Stargardt disease.
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article scientifique
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articolo scientifico
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bilimsel makale
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scientific article published on 03 April 2009
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vetenskaplig artikel
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Novel ABCA4 compound heterozyg ...... esenting as Stargardt disease.
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Novel ABCA4 compound heterozyg ...... esenting as Stargardt disease.
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type
label
Novel ABCA4 compound heterozyg ...... esenting as Stargardt disease.
@en
Novel ABCA4 compound heterozyg ...... esenting as Stargardt disease.
@nl
prefLabel
Novel ABCA4 compound heterozyg ...... esenting as Stargardt disease.
@en
Novel ABCA4 compound heterozyg ...... esenting as Stargardt disease.
@nl
P2093
P2860
P1433
P1476
Novel ABCA4 compound heterozyg ...... resenting as Stargardt disease
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P2093
Elias I Traboulsi
Qing Kenneth Wang
Quansheng Xi
P2860
P304
P577
2009-04-03T00:00:00Z