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1.
Clinical, genetic profile and disease progression of sarcoglycanopathies in a large cohort from India: high prevalence of SGCB c.544A > C.
Neurogenetics
; 23(3): 187-202, 2022 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-35416532
2.
Whole-exome analyses of congenital muscular dystrophy and congenital myopathy patients from India reveal a wide spectrum of known and novel mutations.
Eur J Neurol
; 28(3): 992-1003, 2021 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-33124102
3.
Identification of a shared, common haplotype segregating with an SGCB c.544 T > G mutation in Indian patients affected with sarcoglycanopathy.
Sci Rep
; 13(1): 15095, 2023 09 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-37699968
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