Wheeler MT

References (3)

Title : RAPSN-Associated Congenital Myasthenic Syndrome due to Biallelic Single Nucleotide Variants at the Same Position - Keehan_2025_Case.Rep.Genet_2025_1882021
Author(s) : Keehan L , Carter JN , Kravets E , Wheeler MT , Bernstein JA , Maselli RA , Sampson JB , Bachir S
Ref : Case Rep Genet , 2025 :1882021 , 2025
Abstract :
PubMedSearch : Keehan_2025_Case.Rep.Genet_2025_1882021
PubMedID: 41158980

Title : RAPSN-Associated Congenital Myasthenic Syndrome due to Biallelic Single Nucleotide Variants at the Same Position - Keehan_2025_Case.Rep.Genet_2025_1882021
Author(s) : Keehan L , Carter JN , Kravets E , Wheeler MT , Bernstein JA , Maselli RA , Sampson JB , Bachir S
Ref : Case Rep Genet , 2025 :1882021 , 2025
Abstract :
PubMedSearch : Keehan_2025_Case.Rep.Genet_2025_1882021
PubMedID: 41158980

Title : RAPSN-Associated Congenital Myasthenic Syndrome due to Biallelic Single Nucleotide Variants at the Same Position - Keehan_2025_Case.Rep.Genet_2025_1882021
Author(s) : Keehan L , Carter JN , Kravets E , Wheeler MT , Bernstein JA , Maselli RA , Sampson JB , Bachir S
Ref : Case Rep Genet , 2025 :1882021 , 2025
Abstract :
PubMedSearch : Keehan_2025_Case.Rep.Genet_2025_1882021
PubMedID: 41158980