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Results of search for 'au:"Méjécase, C"'
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Authors
Antonio, A
Audo, I
Blanchard, S
Boyard, F
Condroyer, C
Demontant, V
El Shamieh, S
Letexier, M
Michiels, C
Mohand-Saïd, S
Méjécase, C
Sahel, J-A
Saraiva, J-P
Zeitz, C
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Alleles
Carrier Proteins
Codon, Nonsense
Cohort Studies
Cone-Rod Dystrophies
Consanguinity
Exome Sequencing
Eye Proteins
Female
Fluorescein Angiography
Gene Frequency
Genetic Association Studies
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Membrane Proteins
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Your search returned 2 results.
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1.
A novel nonsense variant in REEP6 is involved in a sporadic rod-cone dystrophy case.
[electronic resource]
by
Méjécase, C
Mohand-Saïd, S
El Shamieh, S
Antonio, A
Condroyer, C
Blanchard, S
Letexier, M
Saraiva, J-P
Sahel, J-A
Audo, I
Zeitz, C
Producer:
20190911
In:
Clinical genetics
vol. 93
Online resources:
Available from publisher's website
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No items available.
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2.
ARL2BP mutations account for 0.1% of autosomal recessive rod-cone dystrophies with the report of a novel splice variant.
[electronic resource]
by
Audo, I
El Shamieh, S
Méjécase, C
Michiels, C
Demontant, V
Antonio, A
Condroyer, C
Boyard, F
Letexier, M
Saraiva, J-P
Blanchard, S
Mohand-Saïd, S
Sahel, J-A
Zeitz, C
Producer:
20180316
In:
Clinical genetics
vol. 92
Online resources:
Available from publisher's website
Availability:
No items available.
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(remove)