Výsledky vyhledávání - "Naderah Da'amseh"

Infantile neurodegenerative disorder associated with mutations in TBCD, an essential gene in the tubulin heterodimer assembly pathway

Autor: Adi Aran, Saiuj Bhat, Nicholas J. Cowan, Hannah Vanyai, Muhannad Daana, Naderah Da'amseh, Julian Ik-Tsen Heng, Guoling Tian, Linh Ngo, Hayley Daniella Cullen, Bassam Abu-Libdeh, Shimon Edvardson, Orly Elpeleg

Publikováno v: Human molecular genetics. 25(21)

Mutation in a growing spectrum of genes is known to either cause or contribute to primary or secondary microcephaly. In primary microcephaly the genetic determinants frequently involve mutations that contribute to or modulate the microtubule cytoskel

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6fd2959dd9b63f5647fa9513c79a599f
https://pubmed.ncbi.nlm.nih.gov/28158450

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