MYH7 mutation identified by next-generation sequencing in three infant siblings with bi-ventricular noncompaction presenting with restrictive hemodynamics: A report of three siblings with a severe phenotype and poor prognosis
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MYH7 mutation identified by next-generation sequencing in three infant siblings with bi-ventricular noncompaction presenting with restrictive hemodynamics: A report of three siblings with a severe phenotype and poor prognosis
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wetenschappelijk artikel
@nl
наукова стаття, опублікована у квітні 2019
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name
MYH7 mutation identified by ne ...... e phenotype and poor prognosis
@en
MYH7 mutation identified by ne ...... e phenotype and poor prognosis
@nl
type
label
MYH7 mutation identified by ne ...... e phenotype and poor prognosis
@en
MYH7 mutation identified by ne ...... e phenotype and poor prognosis
@nl
prefLabel
MYH7 mutation identified by ne ...... e phenotype and poor prognosis
@en
MYH7 mutation identified by ne ...... e phenotype and poor prognosis
@nl
P2093
P921
P1476
MYH7 mutation identified by ne ...... e phenotype and poor prognosis
@en
P2093
Etsuro Ito
Fumitake Miura
Hiroki Mizukami
Jun Shimada
Katsuki Otani
Susumu Yonesaka
Takumi Sato
Toru Takahashi
Tsutomu Toki
Yosuke Kitagawa
P304
P356
10.1016/J.JCCASE.2018.12.017
P407
P577
2019-04-01T00:00:00Z