First molecular study in Lebanese patients with Cockayne syndrome and report of a novel mutation in ERCC8 gene
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First molecular study in Lebanese patients with Cockayne syndrome and report of a novel mutation in ERCC8 gene
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article
@en
wetenschappelijk artikel
@nl
наукова стаття, опублікована у вересні 2018
@uk
name
First molecular study in Leban ...... a novel mutation in ERCC8 gene
@en
First molecular study in Leban ...... a novel mutation in ERCC8 gene
@nl
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First molecular study in Leban ...... a novel mutation in ERCC8 gene
@en
First molecular study in Leban ...... a novel mutation in ERCC8 gene
@nl
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First molecular study in Leban ...... a novel mutation in ERCC8 gene
@en
First molecular study in Leban ...... a novel mutation in ERCC8 gene
@nl
P2093
P2860
P1433
P1476
First molecular study in Leban ...... a novel mutation in ERCC8 gene
@en
P2093
André Megarbane
Cybel Mehawej
Eliane Chouery
Joelle Abou Ghoch
Sandra Corbani
P2860
P2888
P356
10.1186/S12881-018-0677-7
P407
P50
P577
2018-09-10T00:00:00Z
P6179
1106911415