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Akademický článek
Novel mutation in ENG gene causing Hereditary Hemorrhagic Telangiectasia in a Peruvian family
Autor: Alejandro Zevallos-Morales, Alexis Murillo, Milagros M. Dueñas-Roque, Ana Prötzel, Luis Venegas-Tresierra, Verónica Ángeles-Villalba, Miguel Guevara-Cruz, Ada Chávez-Gil, Ricardo Fujita, Maria L. Guevara-Fujita
Publikováno v: Genetics and Molecular Biology, Vol 43, Iss 1 (2020)
Abstract Hereditary Hemorrhagic Telangiectasia (HHT) is a rare disorder of vascular development. Common manifestations include epistaxis, telangiectasias and arteriovenous malformations (AVMs) in multiple organs. Most patients have deletions or misse
Externí odkaz: https://doaj.org/article/5a645b9352d549dbb2382a5638912a93
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2
Novel mutation in ENG gene causing Hereditary Hemorrhagic Telangiectasia in a Peruvian family
Autor: Ana Protzel, Ada Chávez-Gil, María Luisa Guevara-Fujita, Luis Venegas-Tresierra, Milagros M. Dueñas-Roque, Alexis Murillo, Verónica Ángeles-Villalba, Alejandro Zevallos-Morales, Ricardo Fujita, Miguel Guevara-Cruz
Publikováno v: Repositorio Académico USMP
Universidad San Martín de Porres-USMP
USMP-Institucional
Universidad de San Martín de Porres
instacron:USMP
Genetics and Molecular Biology
Genetics and Molecular Biology, Volume: 43, Issue: 1, Article number: e20190126, Published: 27 FEB 2020
Genetics and Molecular Biology, Vol 43, Iss 1 (2020)
Hereditary Hemorrhagic Telangiectasia (HHT) is a rare disorder of vascular development. Common manifestations include epistaxis, telangiectasias and arteriovenous malformations (AVMs) in multiple organs. Most patients have deletions or missense mutat
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::244c4c541935423971b4c0a6a88ff719
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Plný text Recenzováno Digitální knihovna AV ČR
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