Association of De Novo RNF213 Variants With Childhood Onset Moyamoya Disease and Diffuse Occlusive Vasculopathy
Objective To test the hypothesis that de novo genetic variants are responsible for moyamoya
disease (MMD) in children with unaffected relatives, we performed exome sequencing of 28 …
disease (MMD) in children with unaffected relatives, we performed exome sequencing of 28 …
[HTML][HTML] Association of De Novo RNF213 Variants With Childhood Onset Moyamoya Disease and Diffuse Occlusive Vasculopathy
A Pinard, MDJ Fiander, AC Cecchi, AL Rideout… - Neurology, 2021 - ncbi.nlm.nih.gov
Objective To test the hypothesis that de novo genetic variants are responsible for moyamoya
disease (MMD) in children with unaffected relatives, we performed exome sequencing of 28 …
disease (MMD) in children with unaffected relatives, we performed exome sequencing of 28 …
Association of de novo RNF213 variants with childhood onset moyamoya disease and diffuse occlusive vasculopathy.
amélie Pinard, MDJ Fiander, AC Cecchi, AL Rideout… - 2021 - cabidigitallibrary.org
Objective: To test the hypothesis that de novo genetic variants are responsible for
moyamoya disease (MMD) in children with unaffected relatives, we performed exome …
moyamoya disease (MMD) in children with unaffected relatives, we performed exome …
Association of De Novo RNF213 Variants With Childhood Onset Moyamoya Disease and Diffuse Occlusive Vasculopathy
A Pinard, MDJ Fiander, AC Cecchi, AL Rideout… - Neurology, 2021 - cir.nii.ac.jp
抄録< jats: sec>< jats: title> Objective</jats: title>< jats: p> To test the hypothesis that de
novo genetic variants are responsible for moyamoya disease (MMD) in children with …
novo genetic variants are responsible for moyamoya disease (MMD) in children with …
Association of De Novo RNF213 Variants With Childhood Onset Moyamoya Disease and Diffuse Occlusive Vasculopathy.
A Pinard, MDJ Fiander, AC Cecchi, AL Rideout… - Neurology, 2021 - europepmc.org
Objective To test the hypothesis that de novo genetic variants are responsible for moyamoya
disease (MMD) in children with unaffected relatives, we performed exome sequencing of 28 …
disease (MMD) in children with unaffected relatives, we performed exome sequencing of 28 …
Association of De Novo RNF213 Variants With Childhood Onset Moyamoya Disease and Diffuse Occlusive Vasculopathy
A Pinard, MDJ Fiander, AC Cecchi… - …, 2021 - pubmed.ncbi.nlm.nih.gov
Objective To test the hypothesis that de novo genetic variants are responsible for moyamoya
disease (MMD) in children with unaffected relatives, we performed exome sequencing of 28 …
disease (MMD) in children with unaffected relatives, we performed exome sequencing of 28 …
Association of De Novo RNF213 Variants With Childhood Onset Moyamoya Disease and Diffuse Occlusive Vasculopathy.
A Pinard, MDJ Fiander, AC Cecchi, AL Rideout… - Neurology, 2021 - europepmc.org
Objective To test the hypothesis that de novo genetic variants are responsible for moyamoya
disease (MMD) in children with unaffected relatives, we performed exome sequencing of 28 …
disease (MMD) in children with unaffected relatives, we performed exome sequencing of 28 …