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Q33632286-191F42F6-EE3B-4DEF-8146-1413CE1304B9
Q33632286-191F42F6-EE3B-4DEF-8146-1413CE1304B9
BestRank
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http://www.wikidata.org/entity/statement/Q33632286-191F42F6-EE3B-4DEF-8146-1413CE1304B9
Two patients with Hermansky Pudlak syndrome type 2 and novel mutations in AP3B1.
P2860
Q33632286-191F42F6-EE3B-4DEF-8146-1413CE1304B9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33632286-191F42F6-EE3B-4DEF-8146-1413CE1304B9
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wasDerivedFrom
b0d68b126a4c054be4f964d18f438a6a24090ef2
P2860
Oculocutaneous albinism, immunodeficiency, hematological disorders, and minor anomalies: a new autosomal recessive syndrome?