Behr's Syndrome is Typically Associated with Disturbed Mitochondrial Translation and Mutations in the C12orf65 Gene
about
A neurodegenerative perspective on mitochondrial optic neuropathiesAdult Onset Leigh Syndrome in the Intensive Care Setting: A Novel Presentation of a C12orf65 Related Mitochondrial Disease.Genetic heterogeneity of motor neuropathiesReply: Early-onset Behr syndrome due to compound heterozygous mutations in OPA1.
P2860
Behr's Syndrome is Typically Associated with Disturbed Mitochondrial Translation and Mutations in the C12orf65 Gene
description
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name
Behr's Syndrome is Typically A ...... Mutations in the C12orf65 Gene
@ast
Behr's Syndrome is Typically A ...... Mutations in the C12orf65 Gene
@en
type
label
Behr's Syndrome is Typically A ...... Mutations in the C12orf65 Gene
@ast
Behr's Syndrome is Typically A ...... Mutations in the C12orf65 Gene
@en
prefLabel
Behr's Syndrome is Typically A ...... Mutations in the C12orf65 Gene
@ast
Behr's Syndrome is Typically A ...... Mutations in the C12orf65 Gene
@en
P2093
P2860
P50
P356
P1476
Behr's Syndrome is Typically A ...... Mutations in the C12orf65 Gene
@en
P2093
Agnes Herczegfalvi
Gail Eglon
Jennifer Duff
Konstantinos Douroudis
Marina Bartsakoulia
Robert W Taylor
Tania Smertenko
Venkateswaran Ramesh
Veronika Karcagi
P2860
P356
10.3233/JND-140003
P50
P577
2014-01-01T00:00:00Z