<i>PHOX2B</i> mutations and polyalanine expansions correlate with the severity of the respiratory phenotype and associated symptoms in both congenital and late onset Central Hypoventilation syndrome | NobleBlocks
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PHOX2B mutations and polyalanine expansions correlate with the severity of the respiratory phenotype and associated symptoms in both congenital and late onset Central Hypoventilation syndrome
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Shared by NobleBlocks on Apr 28, 2004 • 12:00 AM UTC