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SOS1 mutations in Noonan syndrome: molecular spectrum, structural insights on pathogenic effects, and genotype-phenotype correlationsPTPN11 gene mutation and severe neonatal hypertrophic cardiomyopathy: what is the link?Co-occurrence of hypertrophic cardiomyopathy and myeloproliferative disorder in a neonate with Noonan syndrome carrying Thr73Ile mutation in PTPN11.
P2860
description
article
@en
im Januar 2005 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована у 2005
@uk
name
Hyperthrophic cardiomyopathy and thePTPN11 gene
@en
Hyperthrophic cardiomyopathy and thePTPN11 gene
@nl
type
label
Hyperthrophic cardiomyopathy and thePTPN11 gene
@en
Hyperthrophic cardiomyopathy and thePTPN11 gene
@nl
prefLabel
Hyperthrophic cardiomyopathy and thePTPN11 gene
@en
Hyperthrophic cardiomyopathy and thePTPN11 gene
@nl
P50
P356
P1476
Hyperthrophic cardiomyopathy and thePTPN11 gene
@en
P2093
Anna Sarkozy
Emanuela Conti
P356
10.1002/AJMG.A.30773
P407
P577
2005-01-01T00:00:00Z