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Hermansky-Pudlak syndrome, type 2 gene causing AP3B1 Identification of a homozygous deletion in the
Hermansky-Pudlak syndrome, type 2 gene causing AP3B1 Identification of a homozygous deletion in the
2010
Christoph Klein
Chozhavendan Rathinam Schaffer
Inga Köllner
Carmela Beger
Reinhard Schilke
Karl Welte
Johannes Jung
Georg Bohn
Anna Allroth
Kaan Boztug
Gudrun Brandes
Inga Sandrock
A Alejandro
Keywords:
AP3B1
Hermansky–Pudlak syndrome
Gene
Cancer research
Biology
Correction
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