[HTML][HTML] Disruption of AP3B1by a chromosome 5 inversion: a new disease mechanism in Hermansky-Pudlak syndrome type 2
ML Jones, SL Murden, C Brooks, V Maloney… - BMC medical …, 2013 - Springer
Abstract Background Hermansky-Pudlak syndrome 2 (HPS2; OMIM# 608233) is a rare,
autosomal recessive disorder caused by loss-of-function genetic variations affecting AP3B1 …
autosomal recessive disorder caused by loss-of-function genetic variations affecting AP3B1 …
[HTML][HTML] Disruption of AP3B1 by a chromosome 5 inversion: a new disease mechanism in Hermansky-Pudlak syndrome type 2
ML Jones, SL Murden, C Brooks, V Maloney… - BMC Medical …, 2013 - ncbi.nlm.nih.gov
Background Hermansky-Pudlak syndrome 2 (HPS2; OMIM# 608233) is a rare, autosomal
recessive disorder caused by loss-of-function genetic variations affecting AP3B1, which …
recessive disorder caused by loss-of-function genetic variations affecting AP3B1, which …
[PDF][PDF] Disruption of AP3B1 by a chromosome 5 inversion: a new disease mechanism in Hermansky-Pudlak syndrome type 2
ML Jones, SL Murden, C Brooks, V Maloney… - 2013 - cyberleninka.org
Abstract Background: Hermansky-Pudlak syndrome 2 (HPS2; OMIM# 608233) is a rare,
autosomal recessive disorder caused by loss-of-function genetic variations affecting AP3B1 …
autosomal recessive disorder caused by loss-of-function genetic variations affecting AP3B1 …
Disruption of AP3B1 by a chromosome 5 inversion: a new disease mechanism in Hermansky-Pudlak syndrome type 2.
ML Jones, SL Murden, C Brooks, V Maloney… - BMC Medical …, 2013 - europepmc.org
Background Hermansky-Pudlak syndrome 2 (HPS2; OMIM# 608233) is a rare, autosomal
recessive disorder caused by loss-of-function genetic variations affecting AP3B1, which …
recessive disorder caused by loss-of-function genetic variations affecting AP3B1, which …
[PDF][PDF] Disruption of AP3B1 by a chromosome 5 inversion: a new disease mechanism in Hermansky-Pudlak syndrome type 2
ML Jones, SL Murden, C Brooks, V Maloney… - 2013 - academia.edu
Abstract Background: Hermansky-Pudlak syndrome 2 (HPS2; OMIM# 608233) is a rare,
autosomal recessive disorder caused by loss-of-function genetic variations affecting AP3B1 …
autosomal recessive disorder caused by loss-of-function genetic variations affecting AP3B1 …
Disruption of AP3B1 by a chromosome 5 inversion: a new disease mechanism in Hermansky-Pudlak syndrome type 2
ML Jones, SL Murden, C Brooks… - BMC Medical …, 2013 - search.proquest.com
Background: Hermansky-Pudlak syndrome 2 (HPS2; OMIM# 608233) is a rare, autosomal
recessive disorder caused by loss-of-function genetic variations affecting AP3B1, which …
recessive disorder caused by loss-of-function genetic variations affecting AP3B1, which …
Disruption of AP3B1 by a chromosome 5 inversion: a new disease mechanism in Hermansky-Pudlak syndrome type 2
ML Jones, SL Murden, C Brooks… - BMC Medical …, 2013 - research-information.bris.ac.uk
BACKGROUND: Hermansky-Pudlak syndrome 2 (HPS2; OMIM# 608233) is a rare,
autosomal recessive disorder caused by loss-of-function genetic variations affecting AP3B1 …
autosomal recessive disorder caused by loss-of-function genetic variations affecting AP3B1 …
Disruption of AP3B1 by a chromosome 5 inversion: a new disease mechanism in Hermansky-Pudlak syndrome type 2
ML Jones, SL Murden, C Brooks… - BMC medical …, 2013 - pubmed.ncbi.nlm.nih.gov
Background Hermansky-Pudlak syndrome 2 (HPS2; OMIM# 608233) is a rare, autosomal
recessive disorder caused by loss-of-function genetic variations affecting AP3B1, which …
recessive disorder caused by loss-of-function genetic variations affecting AP3B1, which …
[PDF][PDF] Disruption of AP3B1 by a chromosome 5 inversion: a new disease mechanism in Hermansky-Pudlak syndrome type 2
ML Jones, SL Murden, C Brooks, V Maloney… - 2013 - scienceopen.com
Abstract Background: Hermansky-Pudlak syndrome 2 (HPS2; OMIM# 608233) is a rare,
autosomal recessive disorder caused by loss-of-function genetic variations affecting AP3B1 …
autosomal recessive disorder caused by loss-of-function genetic variations affecting AP3B1 …
[PDF][PDF] Disruption of AP3B1 by a chromosome 5 inversion: a new disease mechanism in Hermansky-Pudlak syndrome type 2
ML Jones, SL Murden, C Brooks, V Maloney… - 2013 - core.ac.uk
Abstract Background: Hermansky-Pudlak syndrome 2 (HPS2; OMIM# 608233) is a rare,
autosomal recessive disorder caused by loss-of-function genetic variations affecting AP3B1 …
autosomal recessive disorder caused by loss-of-function genetic variations affecting AP3B1 …