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pro vyhledávání: '"H J, McMillan"'
Autor:
D A, Dyment, E, Sell, M R, Vanstone, A C, Smith, D, Garandeau, V, Garcia, S, Carpentier, E, Le Trionnaire, F, Sabourdy, C L, Beaulieu, J A, Schwartzentruber, H J, McMillan, J, Majewski, D E, Bulman, T, Levade, S, Scherer
Publikováno v:
Clinical genetics. 86(6)
Spinal muscular atrophy with progressive myoclonic epilepsy (SMA-PME) is a recently delineated, autosomal recessive condition caused by rare mutations in the N-acylsphingosine amidohydrolase 1 (acid ceramidase) ASAH1 gene. It is characterized by moto
Autor:
H J, McMillan, K E, Wynne-Edwards
Publikováno v:
Biology of reproduction. 59(1)
Siberian (Phodopus sungorus) and Djungarian (P. campbelli) hamsters are phenotypically similar and were long considered subspecies. Progesterone (P4) and prolactin (PRL) changes (determined by repeated sampling of individuals) during the behavioral r