TABLE OF CONTENTS
Volume 54, Issue 6 (June 2009)
Original Articles
A novel mutation in NCF1 in an adult CGD patient with a liver abscess as first presentation
Esther van de Vosse, Annelies van Wengen, Jos A van Geelen, Martin de Boer, Dirk Roos and Jaap T van Dissel
J Hum Genet 54: 313-316; advance online publication, March 27, 2009; doi:10.1038/jhg.2009.24
Association study between single-nucleotide polymorphisms in 199 drug-related genes and commonly measured quantitative traits of 752 healthy Japanese subjects
Akira Saito, Manabu Kawamoto and Naoyuki Kamatani
J Hum Genet 54: 317-323; advance online publication, April 3, 2009; doi:10.1038/jhg.2009.31
Structural modeling of mutant 
-glucosidases resulting in a processing/transport defect in Pompe disease
Kanako Sugawara, Seiji Saito, Masakazu Sekijima, Kazuki Ohno, Youichi Tajima, Marian A Kroos, Arnold J J Reuser and Hitoshi Sakuraba
J Hum Genet 54: 324-330; advance online publication, April 3, 2009; doi:10.1038/jhg.2009.32
TC II deficiency: avoidance of false-negative molecular genetics by RNA-based investigations
Johannes Häberle, Silke Pauli, Christoph Berning, Hans G Koch and Michael Linnebank
J Hum Genet 54: 331-334; advance online publication, April 17, 2009; doi:10.1038/jhg.2009.34
A limited spectrum of phenylalanine hydroxylase mutations is observed in phenylketonuria patients in western Poland and implications for treatment with 6R tetrahydrobiopterin
Steven F Dobrowolski, K Borski, C C Ellingson, R Koch, H L Levy and E W Naylor
J Hum Genet 54: 335-339; advance online publication, May 15, 2009; doi:10.1038/jhg.2009.37
Diverse genetic origin of Indian Muslims: evidence from autosomal STR loci
Muthukrishnan Eaaswarkhanth, Bhawna Dubey, Poorlin Ramakodi Meganathan, Zeinab Ravesh, Faizan Ahmed Khan, Lalji Singh, Kumarasamy Thangaraj and Ikramul Haque
J Hum Genet 54: 340-348; advance online publication, May 8, 2009; doi:10.1038/jhg.2009.38
Revisiting the peopling of Japan: an admixture perspective
Rita Rasteiro and Lounès Chikhi
J Hum Genet 54: 349-354; advance online publication, May 8, 2009; doi:10.1038/jhg.2009.39
Molecular cloning of t(2;7)(p24.3;p14.2), a novel chromosomal translocation in myelodysplastic syndrome-derived acute myeloid leukemia
Kazuhiro Fujita, Masashi Sanada, Hiroshi Harada, Hiraku Mori, Haruo Niikura, Mitsuhiro Omine, Johji Inazawa and Issei Imoto
J Hum Genet 54: 355-359; advance online publication, May 1, 2009; doi:10.1038/jhg.2009.40
Arg347Cys polymorphism of 1A-adrenoceptor gene is associated with blood pressure response to nifedipine GITS in Chinese hypertensive patients
Yan Zhang, Xiumei Hong, Haipeng Liu, Yong Huo and Xiping Xu
J Hum Genet 54: 360-364; advance online publication, May 15, 2009; doi:10.1038/jhg.2009.42
Mutations in the LMNA gene do not cause axonal CMT in Czech patients
Petra La
uthová, Lucia Baránková, Jana Haberlová, Radim Mazanec, Andrew Wallace, Kathrin Huehne, Bernd Rautenstrauss and Pavel Seeman
J Hum Genet 54: 365-368; advance online publication, May 8, 2009; doi:10.1038/jhg.2009.43
MEFV mutation carriage in Israeli Jewish individuals from ethnicities with low risk for familial Mediterranean fever
Olga Feld, Avi Livneh, Yael Shinar, Yaakov Berkun and Merav Lidar
J Hum Genet 54: 369-371; advance online publication, April 17, 2009; doi:10.1038/jhg.2009.33
Short Communication
Frequencies of genotypes and alleles of the functional SNPs in CYP2C19 and CYP2E1 in mainland Chinese Kazakh, Uygur and Han populations
Shu-Mei Wang, An-Ping Zhu, Dan Li, Zhen Wang, Ping Zhang and Guo-Liang Zhang
J Hum Genet 54: 372-375; advance online publication, May 15, 2009; doi:10.1038/jhg.2009.41
