المؤلفون: Safwat, Sylvia^{Aff1, Aff2}, Flannery, Kyle P., El Beheiry, Ahmed A., Mokhtar, Mohamed M., Abdalla, Ebtesam, Manzini, M. Chiara^{Aff1, IDs1004802400745z_cor6}

المصدر: Neurogenetics: New developments in Neurogenetics and Neuroepigenetics.. 25(2):93-102

المؤلفون: Dong-Won Seol, Byoung-Jin Park, Deog-Bon Koo, Ji-Su Kim, Yong-Hyun Jeon, Jae-Eon Lee, Joon-Suk Park, Hoon Jang, Gabbine Wee

المصدر: Current Issues in Molecular Biology, Vol 46, Iss 5, Pp 3752-3762 (2024)

مصطلحات موضوعية: Fukuyama congenital muscular dystrophy, fukutin gene, knockout rat model, CRISPR/Cas9, Biology (General), QH301-705.5

وصف الملف: electronic resource

Relation: https://www.mdpi.com/1467-3045/46/5/234; https://doaj.org/toc/1467-3037; https://doaj.org/toc/1467-3045

URL الوصول: https://doaj.org/article/5880472cb97c461a8900774c54fd234a

المؤلفون: Naghipoor, Karim, Khosravi, Teymoor, Oladnabi, Morteza^{Aff2, Aff3, Aff4, IDs11033023086446_cor3}

المصدر: Molecular Biology Reports: An International Journal on Molecular and Cellular Biology. 50(9):7427-7435

المؤلفون: El Kadiri, Youssef^{Aff1, Aff2, IDs4304202300416y_cor1}, Ratbi, Ilham^{Aff1, Aff2}, Ouhenach, Mouna, Chafai Elalaoui, Siham^{Aff1, Aff2}, Cherkaoui Jaouad, Imane, Zrhidri, Abdelali^{Aff1, Aff2}, Sahli, Maryem, Birouk, Nazha, Sefiani, Abdelaziz^{Aff1, Aff2}, Lyahyai, Jaber^{Aff1, Aff2}

المصدر: Egyptian Journal of Medical Human Genetics. 24(1)

المؤلفون: Manuela Moriggi, Enrica Torretta, Matilde Cescon, Loris Russo, Ilaria Gregorio, Paola Braghetta, Patrizia Sabatelli, Cesare Faldini, Luciano Merlini, Cesare Gargioli, Paolo Bonaldo, Cecilia Gelfi, Daniele Capitanio

المصدر: International Journal of Molecular Sciences, Vol 25, Iss 13, p 7118 (2024)

مصطلحات موضوعية: pericyte, skeletal muscle, myogenic differentiation, muscle aging, Ullrich congenital muscular dystrophy, Bethlem myopathy, Biology (General), QH301-705.5, Chemistry, QD1-999

وصف الملف: electronic resource

Relation: https://www.mdpi.com/1422-0067/25/13/7118; https://doaj.org/toc/1661-6596; https://doaj.org/toc/1422-0067

URL الوصول: https://doaj.org/article/4214af8259e44f6fa471124b64b1c968

المؤلفون: Victor Morel, Frédérique Audic, Charlotte Tardy, Annie Verschueren, Shahram Attarian, Karine Nguyen, Emmanuelle Salort-Campana, Martin Krahn, Brigitte Chabrol, Svetlana Gorokhova

المصدر: Frontiers in Genetics, Vol 14 (2023)

مصطلحات موضوعية: collagen type VI-related myopathies, COL6-RD, Bethlem myopathy, ullrich’s congenital muscular dystrophy, COL6 genes, COL6A1, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fgene.2023.1242277/full; https://doaj.org/toc/1664-8021

URL الوصول: https://doaj.org/article/1022638a6b0345fdaf9d6b75b3f39571

المؤلفون: McMillan, Hugh J^{Aff4, Aff5, Aff6}, Oskoui, Maryam^{Aff5, Aff6}

المساهمون: Tarsy, Daniel, Series Editor^Aff1, Narayanaswami, Pushpa, editor^Aff2, Liewluck, Teerin, editor^Aff3

المصدر: Principles and Practice of the Muscular Dystrophies. :175-191

المؤلفون: Baydan, Figen^Aff2, Tiftikcioglu, Bedile Irem^Aff3, Diniz, Gulden^Aff4

المساهمون: Diniz, Gulden, editor^Aff1

المصدر: Clues for Differential Diagnosis of Neuromuscular Disorders. :183-218

المؤلفون: Hitomi Fujita

المصدر: Pediatric Reports, Vol 15, Iss 3, Pp 403-413 (2023)

مصطلحات موضوعية: power mobility device, Fukuyama congenital muscular dystrophy, psychological effect, assessment of learning powered mobility use tool, early intervention, physical therapy, Medicine, Pediatrics, RJ1-570

وصف الملف: electronic resource

Relation: https://www.mdpi.com/2036-7503/15/3/37; https://doaj.org/toc/2036-7503

URL الوصول: https://doaj.org/article/b78067de1cea4b79b32005534b81e9a8

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