Title : Prevalent LIPH founder mutations lead to loss of P2Y5 activation ability of PA-PLA1alpha in autosomal recessive hypotrichosis - Shinkuma_2010_Hum.Mutat_31_602 |
Author(s) : Shinkuma S , Akiyama M , Inoue A , Aoki J , Natsuga K , Nomura T , Arita K , Abe R , Ito K , Nakamura H , Ujiie H , Shibaki A , Suga H , Tsunemi Y , Nishie W , Shimizu H |
Ref : Hum Mutat , 31 :602 , 2010 |
Abstract : Shinkuma_2010_Hum.Mutat_31_602 |
ESTHER : Shinkuma_2010_Hum.Mutat_31_602 |
PubMedSearch : Shinkuma_2010_Hum.Mutat_31_602 |
PubMedID: 20213768 |
Gene_locus related to this paper: human-LIPH |
Gene_locus related to this paper: human-LIPH |
Shinkuma S, Akiyama M, Inoue A, Aoki J, Natsuga K, Nomura T, Arita K, Abe R, Ito K, Nakamura H, Ujiie H, Shibaki A, Suga H, Tsunemi Y, Nishie W, Shimizu H (2010)
Prevalent LIPH founder mutations lead to loss of P2Y5 activation ability of PA-PLA1alpha in autosomal recessive hypotrichosis
Hum Mutat
31 :602
Shinkuma S, Akiyama M, Inoue A, Aoki J, Natsuga K, Nomura T, Arita K, Abe R, Ito K, Nakamura H, Ujiie H, Shibaki A, Suga H, Tsunemi Y, Nishie W, Shimizu H (2010)
Hum Mutat
31 :602