[HTML][HTML] Spinal muscular atrophy-like phenotype in a mouse model of acid ceramidase deficiency
MS Nagree, J Rybova, A Kleynerman… - Communications …, 2023 - nature.com
Mutations in ASAH1 have been linked to two allegedly distinct disorders: Farber disease
(FD) and spinal muscular atrophy with progressive myoclonic epilepsy (SMA-PME). We …
(FD) and spinal muscular atrophy with progressive myoclonic epilepsy (SMA-PME). We …
Spinal muscular atrophy-like phenotype in a mouse model of acid ceramidase deficiency
MS Nagree, J Rybova, A Kleynerman… - Communications …, 2023 - pubmed.ncbi.nlm.nih.gov
Mutations in ASAH1 have been linked to two allegedly distinct disorders: Farber disease
(FD) and spinal muscular atrophy with progressive myoclonic epilepsy (SMA-PME). We …
(FD) and spinal muscular atrophy with progressive myoclonic epilepsy (SMA-PME). We …
[HTML][HTML] Spinal muscular atrophy-like phenotype in a mouse model of acid ceramidase deficiency
MS Nagree, J Rybova, A Kleynerman… - Communications …, 2023 - ncbi.nlm.nih.gov
Mutations in ASAH1 have been linked to two allegedly distinct disorders: Farber disease
(FD) and spinal muscular atrophy with progressive myoclonic epilepsy (SMA-PME). We …
(FD) and spinal muscular atrophy with progressive myoclonic epilepsy (SMA-PME). We …
Spinal muscular atrophy-like phenotype in a mouse model of acid ceramidase deficiency.
MS Nagree, J Rybova, A Kleynerman… - Communications …, 2023 - europepmc.org
Mutations in ASAH1 have been linked to two allegedly distinct disorders: Farber disease
(FD) and spinal muscular atrophy with progressive myoclonic epilepsy (SMA-PME). We …
(FD) and spinal muscular atrophy with progressive myoclonic epilepsy (SMA-PME). We …
Spinal muscular atrophy-like phenotype in a mouse model of acid ceramidase deficiency
MS Nagree, J Rybova, A Kleynerman… - Communications …, 2023 - search.proquest.com
Mutations in ASAH1 have been linked to two allegedly distinct disorders: Farber disease
(FD) and spinal muscular atrophy with progressive myoclonic epilepsy (SMA-PME). We …
(FD) and spinal muscular atrophy with progressive myoclonic epilepsy (SMA-PME). We …
Spinal muscular atrophy-like phenotype in a mouse model of acid ceramidase deficiency.
MS Nagree, J Rybova, A Kleynerman… - Communications …, 2023 - search.ebscohost.com
Mutations in ASAH1 have been linked to two allegedly distinct disorders: Farber disease
(FD) and spinal muscular atrophy with progressive myoclonic epilepsy (SMA-PME). We …
(FD) and spinal muscular atrophy with progressive myoclonic epilepsy (SMA-PME). We …
Spinal muscular atrophy-like phenotype in a mouse model of acid ceramidase deficiency.
MS Nagree, J Rybova, A Kleynerman… - Communications …, 2023 - europepmc.org
Mutations in ASAH1 have been linked to two allegedly distinct disorders: Farber disease
(FD) and spinal muscular atrophy with progressive myoclonic epilepsy (SMA-PME). We …
(FD) and spinal muscular atrophy with progressive myoclonic epilepsy (SMA-PME). We …