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Duchenne Muscular Dystrophy in Kazakhstan: A Journey from Diagnosis to the Treatment, the Biases and Achievements.
J Neuromuscul Dis. 2023;10(2):263-269. doi: 10.3233/JND-221559.
J Neuromuscul Dis. 2023.
PMID: 36641684
Free PMC article.
Whole-Genome Sequencing Among Kazakhstani Children with Early-Onset Epilepsy Revealed New Gene Variants and Phenotypic Variability.
Bayanova M, Bolatov AK, Bazenova A, Nazarova L, Nauryzbayeva A, Tanko NM, Rakhimova S, Satvaldina N, Samakyzy D, Kozhamkulov U, Kairov U, Akilzhanova A, Sarbassov D.
Bayanova M, et al.
Mol Neurobiol. 2023 Aug;60(8):4324-4335. doi: 10.1007/s12035-023-03346-3. Epub 2023 Apr 24.
Mol Neurobiol. 2023.
PMID: 37095367
Free PMC article.
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Delayed Diagnosis of Perrault Syndrome: A Rare Genetic Disorder.
Bayanova M, Abilova A, Nauryzbayeva A, Turarbekova Z.
Bayanova M, et al.
Case Rep Med. 2024 Jan 12;2024:5319443. doi: 10.1155/2024/5319443. eCollection 2024.
Case Rep Med. 2024.
PMID: 38249302
Free PMC article.
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