A novel double nucleotide variant in the ferritin-L iron-responsive element in a Finnish patient with hereditary hyperferritinaemia-cataract syndrome.
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A novel double nucleotide variant in the ferritin-L iron-responsive element in a Finnish patient with hereditary hyperferritinaemia-cataract syndrome.
description
2017 nî lūn-bûn
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2017年の論文
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name
A novel double nucleotide vari ...... rritinaemia-cataract syndrome.
@en
A novel double nucleotide vari ...... rritinaemia-cataract syndrome.
@nl
type
label
A novel double nucleotide vari ...... rritinaemia-cataract syndrome.
@en
A novel double nucleotide vari ...... rritinaemia-cataract syndrome.
@nl
prefLabel
A novel double nucleotide vari ...... rritinaemia-cataract syndrome.
@en
A novel double nucleotide vari ...... rritinaemia-cataract syndrome.
@nl
P2093
P2860
P356
P1433
P1476
A novel double nucleotide vari ...... rritinaemia-cataract syndrome.
@en
P2093
Juha Pursiheimo
Marketta Järveläinen
Roosa-Maria Mattila
P2860
P356
10.1111/AOS.13492
P577
2017-06-21T00:00:00Z