المؤلفون: Wei Zheng, Ji He, Lu Chen, Weiyi Yu, Nan Zhang, Xiaoxuan Liu, Dongsheng Fan

المصدر: Frontiers in Aging Neuroscience, Vol 16 (2024)

مصطلحات موضوعية: amyotrophic lateral sclerosis, KIF1A, axonal transport, KIF5A, cosegregation analysis, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fnagi.2024.1421841/full; https://doaj.org/toc/1663-4365

URL الوصول: https://doaj.org/article/d8b06ea173d84e07afda6c916ad05c64

المؤلفون: Olga S. Chumakova, Svetlana N. Nasonova, Yulia V. Frolova, Elena A. Stepanova, Elena A. Mershina, Valentin E. Sinitsyn, Dmitry A. Zateyshchikov, Igor V. Zhirov

المصدر: Терапевтический архив, Vol 95, Iss 4, Pp 335-340 (2023)

مصطلحات موضوعية: amyloidosis, transthyretin, hereditary, pathogenicity, variant, p.e112k, gene, cosegregation, phenotype, ethanol, Medicine

وصف الملف: electronic resource

Relation: https://ter-arkhiv.ru/0040-3660/article/viewFile/472052/125352; https://doaj.org/toc/0040-3660; https://doaj.org/toc/2309-5342

URL الوصول: https://doaj.org/article/fecf7548b13245a8b80d787b1192c960

المؤلفون: Belman, Sophie^{Aff1, Aff3}, Parsons, Michael T., Spurdle, Amanda B., Goldgar, David E., Feng, Bing-Jian^Aff1

المصدر: Genetics in Medicine: Official journal of the American College of Medical Genetics and Genomics. 22(12):2052-2059

المؤلفون: Silje Anda, Erik Boye, Kay Oliver Schink, Beata Grallert

المصدر: Open Biology, Vol 11, Iss 8 (2021)

مصطلحات موضوعية: cosegregation, asymmetric segregation, spindle pole body, DNA segregation, Biology (General), QH301-705.5

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2046-2441

URL الوصول: https://doaj.org/article/387cccee37c94c93bcaf07c1ed968df5

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المؤلفون: Tranel, Patrick J., Wu, Chenxi, Sadeque, Ahmed

المصدر: Weed Science, 2017 Jan 01. 65(1), 4-8.

URL الوصول: https://www.jstor.org/stable/26420794

المؤلفون: Vooijs, Riet, Schat, Henk

المصدر: The New Phytologist, 2003 Aug 01. 159(2), 383-390.

URL الوصول: https://www.jstor.org/stable/1514234

المؤلفون: Pomares, Esther^{Aff1_43, Aff2_43, Aff3_43}, Marfany, Gemma^{Aff1_43, Aff2_43, Aff3_43}, Gonzàlez-Duarte, Roser^{Aff1_43, Aff2_43, Aff3_43}

المساهمون: LaVail, Matthew M., editor^AffID1, Ash, John D., editor^AffID2, Anderson, Robert E., editor^AffID3, Hollyfield, Joe G., editor^AffID4, Grimm, Christian, editor^AffID5

المصدر: Retinal Degenerative Diseases. 723:329-335

المؤلفون: Yun Li, Ruth Sheffer, Peter Nürnberg, Muhannad Daana, Silke Kaulfuss, Hagar Mor-Shakad, Bernd Wollnik, Janine Altmüller, Knut Brockmann, Peter Burfeind, Emrah Kaygusuz, Liza Douiev, Gökhan Yigit

المصدر: Journal of Medical Genetics. 59:549-553

مصطلحات موضوعية: Genetics, 0303 health sciences, Mutation, Cosegregation, Genetic heterogeneity, media_common.quotation_subject, Nonsense, Biology, medicine.disease_cause, medicine.disease, 03 medical and health sciences, Epilepsy, 0302 clinical medicine, medicine, Missense mutation, Gene, 030217 neurology & neurosurgery, Genetics (clinical), Loss function, 030304 developmental biology, media_common

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::071e868fe3d7984d7b7e5275445c4f05
https://doi.org/10.1136/jmedgenet-2021-107769