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Whole Exome Sequencing Identifies De Novo HRAS Mutation Underlying Primary IGF1 Deficiency (PIGFD)
Whole Exome Sequencing Identifies De Novo HRAS Mutation Underlying Primary IGF1 Deficiency (PIGFD)
2015
Greta Grosse
Alina C. Hilger
Markus Draaken
Michael Ludwig
Heiko Reutter
Franziska Lorenzen
Joachim Woelfle
Keywords:
HRAS
Exome
Exome sequencing
IGF1 Deficiency
Genetics
Biology
Mutation
Correction
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