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Items: 3

1.
A novel de novo variant of LAMA2 contributes to merosin deficient congenital muscular dystrophy type 1A: Case report
Kien Trung Tran, Vinh Sy Le, Chinh Duy Vu, Liem Thanh Nguyen
Biomed Rep. 2020 Feb; 12(2): 46–50. Published online 2019 Nov 27. doi: 10.3892/br.2019.1260
PMCID:
PMC6951223
AbstractArticlePDF–626K
2.
Universal Primers as a Potential Tool for the Detection of Emerging Flaviviruses
Iván Delgado-Enciso, Francisco Espinoza-Gómez, Erika J Verján-Carrillo, Gabriel Ceja-Espiritu, Perla A Rios-Flores, Tiburcio Lizama-Munguía, Jorge A Salazar-Barragán, Jose B Soto-Castellano, Salvador Valle-Reyes, Uriel A López-Lemus
J Glob Infect Dis. 2019 Jul-Sep; 11(3): 127–129. doi: 10.4103/jgid.jgid_137_18
PMCID:
PMC6733189
ArticlePDF–255K
3.
Rare variant in LAMA2 gene causing congenital muscular dystrophy in a Sudanese family. A case report
MUTAZ AMIN, YOUSUF BAKHIT, MAHMOUD KOKO, MOHAMED OSAMA MIRGAHNI IBRAHIM, MA SALIH, MUNTASER IBRAHIM, OSHEIK A SEIDI
Acta Myol. 2019 Mar; 38(1): 21–24. Published online 2019 Mar 1.
PMCID:
PMC6598405
AbstractArticlePDF–133K

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