The detail information of Muscular dystrophy, limb-girdle, type R3 (LGMDR3)
OMIA Basic Information

Possible human homologues (MIM numbers):

Mendelian trait/disorder: yes

Mode of inheritance: Autosomal Recessive

Considered a defect: yes

Year key mutation first reported: 2021

Species-specific name: -

Species-specific symbol: -

More detail information can see in

Associated Breeds
There are associated breeds.
Associated Gene
There are no associated genes.
References
Note: the references are listed in reverse chronological order (from the most recent year to the earliest year), and alphabetically by first author within a year.
2021 Mickelson,J.R.,Minor,K.M.,Guo,L.T.,Friedenberg,S.G.,Cullen,J.N.,Ciavarella,A.,Hambrook,L.E.,Brenner,K.M.,Helmond,S.E.,Marks,S.L.,Shelton,G.D.: :
Sarcoglycan A mutation in miniature dachshund dogs causes limb-girdle muscular dystrophy 2D. Skelet Muscle 11:2, 2021.
Pubmed reference: 33407862 . DOI: 10.1186/s13395-020-00257-y .