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UnknownHomozygous mutations in NEUROD1 are responsible for a novel syndrome of permanent neonatal diabetes and neurological abnormalities.
Not available
S-EPMC2927956 | biostudies-literature
UnknownPermanent Neonatal Diabetes and Enteric Anendocrinosis Associated With Biallelic Mutations in NEUROG3.
Not available
S-EPMC3064109 | biostudies-literature
UnknownClinical heterogeneity in patients with FOXP3 mutations presenting with permanent neonatal diabetes.
Not available
S-EPMC2606841 | biostudies-literature
UnknownAnalysis of transcription factors key for mouse pancreatic development establishes NKX2-2 and MNX1 mutations as causes of neonatal diabetes in man.
Not available
S-EPMC3887257 | biostudies-literature
UnknownIdentification of a pathogenic mutation in <i>ARPP21</i> in patients with amyotrophic lateral sclerosis.
Not available
S-EPMC11877019 | biostudies-literature
UnknownPartial lipodystrophy and insulin resistant diabetes in a patient with a homozygous nonsense mutation in CIDEC.
Not available
S-EPMC2891108 | biostudies-literature
UnknownLymphovascular Space Invasion in Early-Stage Endometrial Cancer (LySEC): Patterns of Recurrence and Predictors. A Multicentre Retrospective Cohort Study of the Spain Gynecologic Oncology Group.
Not available
S-EPMC10177148 | biostudies-literature
UnknownRecessive mutations in the INS gene result in neonatal diabetes through reduced insulin biosynthesis.
Not available
S-EPMC2840338 | biostudies-literature
UnknownGATA6 haploinsufficiency causes pancreatic agenesis in humans.
Not available
S-EPMC4062962 | biostudies-literature
UnknownWolcott-Rallison syndrome is the most common genetic cause of permanent neonatal diabetes in consanguineous families.
Not available
S-EPMC2775655 | biostudies-literature
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