A. Allroth
发表
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The New England journal of medicine.
Identification of a homozygous deletion in the AP3B1 gene causing Hermansky-Pudlak syndrome, type 2.
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A. Schäffer,
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A. Schäffer,
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Bodo Grimbacher,
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Nature Medicine.
A. Schäffer,
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2022
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A A Schäffer,
M Perro,
C Woellner,
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