Clinical features of neurodegeneration with brain iron accumulation due to a C19orf12 gene mutation.
about
Impairment of Drosophila orthologs of the human orphan protein C19orf12 induces bang sensitivity and neurodegenerationNeurodegeneration with brain iron accumulation: diagnosis and managementPathophysiology and treatment of neurodegeneration with brain iron accumulation in the pediatric population.Clinical and imaging characteristics of late onset mitochondrial membrane protein-associated neurodegeneration (MPAN)
P2860
Clinical features of neurodegeneration with brain iron accumulation due to a C19orf12 gene mutation.
description
2013 nî lūn-bûn
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name
Clinical features of neurodege ...... e to a C19orf12 gene mutation.
@en
Clinical features of neurodege ...... e to a C19orf12 gene mutation.
@nl
type
label
Clinical features of neurodege ...... e to a C19orf12 gene mutation.
@en
Clinical features of neurodege ...... e to a C19orf12 gene mutation.
@nl
prefLabel
Clinical features of neurodege ...... e to a C19orf12 gene mutation.
@en
Clinical features of neurodege ...... e to a C19orf12 gene mutation.
@nl
P2093
P2860
P356
P1433
P1476
Clinical features of neurodege ...... e to a C19orf12 gene mutation.
@en
P2093
Allison Gregory
Elizabeth Berry-Kravis
Jennifer G Goldman
Penelope Hogarth
Sheila R Eichenseer
Simon Zimnowodzki
Susan J Hayflick
P2860
P304
P356
10.1002/MDS.25410
P407
P577
2013-03-13T00:00:00Z