Значок книги

Hereditary Retinopathies Progress in Development of Genetic and Molecular Therapies /

The hereditary retinopathy, retinitis pigmentosa (RP), which affects 1 in 3,500 people worldwide, is the most common cause of registered visual handicap among those of the working age in developed countries. RP is a highly variable disorder where patients may develop symptomatic visual loss in early...

Полное описание

Сохранить в:
Библиографические подробности
Главные авторы: Humphries, Pete. (Автор, http://id.loc.gov/vocabulary/relators/aut), Humphries, Marian M. (http://id.loc.gov/vocabulary/relators/aut), Tam, Lawrence C. S. (http://id.loc.gov/vocabulary/relators/aut), Farrar, G. Jane. (http://id.loc.gov/vocabulary/relators/aut), Kenna, Paul F. (http://id.loc.gov/vocabulary/relators/aut), Campbell, Matthew. (http://id.loc.gov/vocabulary/relators/aut), Kiang, Anna-Sophia. (http://id.loc.gov/vocabulary/relators/aut)
Соавтор: SpringerLink (Online service)
Формат: Электронный ресурс eКнига
Язык:English
Опубликовано: New York, NY : Springer New York : Imprint: Springer, 2012.
Редактирование:1st ed. 2012.
Серии:SpringerBriefs in Genetics, 1
Предметы:
Human genetics.
Gene therapy.
Ophthalmology.
Human Genetics.
Gene Therapy.
Online-ссылка:https://doi.org/10.1007/978-1-4614-4499-2
Метки: Добавить метку
Нет меток, Требуется 1-ая метка записи!

Internet

https://doi.org/10.1007/978-1-4614-4499-2

Схожие документы