bibliographic resource 341166 [br/341166]
https://w3id.org/oc/corpus/br/341166

is a

• document
• article

title

• SCN9A Mutations in Paroxysmal Extreme Pain Disorder: Allelic Variants Underlie Distinct Channel Defects and Phenotypes

publication date

• 2006-01-01

contributor

• https://w3id.org/oc/corpus/ar/986387
• https://w3id.org/oc/corpus/ar/986388
• https://w3id.org/oc/corpus/ar/986389
• https://w3id.org/oc/corpus/ar/986390
• https://w3id.org/oc/corpus/ar/986391
• https://w3id.org/oc/corpus/ar/986392
• https://w3id.org/oc/corpus/ar/986393
• https://w3id.org/oc/corpus/ar/986394
• https://w3id.org/oc/corpus/ar/986395
• https://w3id.org/oc/corpus/ar/986396
• https://w3id.org/oc/corpus/ar/986397
• https://w3id.org/oc/corpus/ar/986398

format

• https://w3id.org/oc/corpus/re/132171

identifier

• https://w3id.org/oc/corpus/id/14585715
• https://w3id.org/oc/corpus/id/507429
• https://w3id.org/oc/corpus/id/507430
• https://w3id.org/oc/corpus/id/507431

part of

• https://w3id.org/oc/corpus/br/341167