The mutational spectrum of holoprosencephaly-associated changes within the SHH gene in humans predicts loss-of-function through either key structural alterations of the ligand or its altered synthesis

author
created [InstanceEdit:5358248] Rothfels, Karen, 2014年03月27日
dbId 5358247
displayName The mutational spectrum of holoprosencephaly-associated changes within the SHH gene in humans predicts loss-of-function through either key structural alterations of the ligand or its altered synthesis
journal Hum. Mutat.
pages E921-35
pubMedIdentifier 19603532
schemaClass LiteratureReference
title The mutational spectrum of holoprosencephaly-associated changes within the SHH gene in humans predicts loss-of-function through either key structural alterations of the ligand or its altered synthesis
url http://www.ncbi.nlm.nih.gov/pubmed/19603532
volume 30
year 2009

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