Open AccessReply: Autosomal dominant segregation of CAPN3 c.598_612del15 associated with a mild form of calpainopathy
Author(s) -
Nallamilli Babi Ramesh Reddy,
Chakravorty Samya,
Kesari Akanchha,
Bean Lora,
Hegde Madhuri
Publication year - 2020
Publication title -
annals of clinical and translational neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.824
H-Index - 42
ISSN - 2328-9503
DOI - 10.1002/acn3.51192
Subject(s) - missense mutation , phenotype , genetics , medicine , genotype , gene , biology