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Exome sequencing reveals a pallidin mutation in a Hermansky-Pudlak-like primary immunodeficiency syndrome.

Badolato R
•
PRANDINI, ALBERTO
•
Caracciolo S
altro
Kingsmore S.F.
2012
  • journal article

Periodico
BLOOD
Archivio
http://hdl.handle.net/11368/2602824
http://hdl.handle.net/11368/2592221
info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84859330854
http://www.ncbi.nlm.nih.gov/pubmed/22461475
Diritti
metadata only access
Soggetti
  • PLDN protein

  • Hermanski-Pudlak Synd...

  • exome sequencing

  • partial albinism

Scopus© citazioni
53
Data di acquisizione
Jun 7, 2022
Vedi dettagli
Visualizzazioni
3
Data di acquisizione
Apr 19, 2024
Vedi dettagli
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