Pigmentation, pleiotropy, and genetic pathways in humans and mice.
about
Waardenburg syndromeEvidence for a retroviral insertion in TRPM1 as the cause of congenital stationary night blindness and leopard complex spotting in the horse.Characterization of genes modulated during pheomelanogenesis using differential displayThe ocular albinism type 1 gene product is a membrane glycoprotein localized to melanosomes
P2860
Pigmentation, pleiotropy, and genetic pathways in humans and mice.
description
1995 nî lūn-bûn
@nan
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
1995年论文
@zh
1995年论文
@zh-cn
name
Pigmentation, pleiotropy, and genetic pathways in humans and mice.
@en
Pigmentation, pleiotropy, and genetic pathways in humans and mice.
@nl
type
label
Pigmentation, pleiotropy, and genetic pathways in humans and mice.
@en
Pigmentation, pleiotropy, and genetic pathways in humans and mice.
@nl
prefLabel
Pigmentation, pleiotropy, and genetic pathways in humans and mice.
@en
Pigmentation, pleiotropy, and genetic pathways in humans and mice.
@nl
P2860
P1476
Pigmentation, pleiotropy, and genetic pathways in humans and mice.
@en
P2093
P2860
P304
P407
P577
1995-10-01T00:00:00Z