De novo variant in KIF26B is associated with pontocerebellar hypoplasia with infantile spinal muscular atrophy
American Journal of Medical Genetics Part A, EarlyView.
Source: American Journal of Medical Genetics Part A - Category: Genetics & Stem Cells Authors: Monica H.
Wojcik
,
Kyoko
Okada
,
Sanjay P.
Prabhu
,
Dan W.
Nowakowski
,
Keri
Ramsey
,
Chris
Balak
,
Sampath
Rangasamy
,
Catherine A.
Brownstein
,
Klaus
Schmitz ‐Abe
,
Julie S.
Cohen
,
Ali
Fatemi
,
Jiahai
Shi
Source Type: research
More News: Genetics | Spinal Muscular Atrophy