Open Access UCL Research: Exome reanalysis and proteomic profiling identified TRIP4 as a novel cause of cerebellar hypoplasia and spinal muscular atrophy (PCH1) https://t.co/QiY1FKf67B
RT @ejhg_journal: TRIP4 as a novel cause of a spinal muscular atrophy phenotype https://t.co/ugrrub6be7
RT @ejhg_journal: TRIP4 as a novel cause of a spinal muscular atrophy phenotype https://t.co/ugrrub6be7
TRIP4 as a novel cause of a spinal muscular atrophy phenotype https://t.co/ugrrub6be7
(備忘録)後で読む Exome reanalysis and proteomic profiling identified TRIP4 as a novel cause of cerebellar hypoplasia and spinal muscular atrophy (PCH1). https://t.co/n2ZWh3LW8W
RT @HorvathLab: ❗️❗️We identified TRIP4 as a novel variant causing cerebellar hypoplasia and spinal muscular atrophy! Many thanks to all c…
RT @Solve_RD: In the @euro_nmd case report Ana Topf et al. from @jwmdrc @UniofNewcastle identified TRIP4 as a novel cause of cerebellar hy…
RT @Solve_RD: In the @euro_nmd case report Ana Topf et al. from @jwmdrc @UniofNewcastle identified TRIP4 as a novel cause of cerebellar hy…
RT @Solve_RD: In the @euro_nmd case report Ana Topf et al. from @jwmdrc @UniofNewcastle identified TRIP4 as a novel cause of cerebellar hy…
RT @HorvathLab: ❗️❗️We identified TRIP4 as a novel variant causing cerebellar hypoplasia and spinal muscular atrophy! Many thanks to all c…
RT @HorvathLab: ❗️❗️We identified TRIP4 as a novel variant causing cerebellar hypoplasia and spinal muscular atrophy! Many thanks to all c…
❗️❗️We identified TRIP4 as a novel variant causing cerebellar hypoplasia and spinal muscular atrophy! Many thanks to all collaborators! https://t.co/NwaS5qjT8u
RT @Solve_RD: In the @euro_nmd case report Ana Topf et al. from @jwmdrc @UniofNewcastle identified TRIP4 as a novel cause of cerebellar hy…
In the @euro_nmd case report Ana Topf et al. from @jwmdrc @UniofNewcastle identified TRIP4 as a novel cause of cerebellar hypoplasia and spinal muscular atrophy by exome reanalysis and proteomic profiling. @TeresinhaEvange @HorvathLab @VolkerWStraub htt