PRM1 variant rs35576928 (Arg>Ser) is associated with defective spermatogenesis in the Chinese Han population

Reproductive BioMedicine Online

Volumn 25, Issue 6, 2012, Pages 627-634

  He, Xiao Jin ^a   Ruan, Jian ^a   Du, Wei Dong ^a,b   Chen, Gang ^a   Zhou, Yuan ^a   Xu, Song ^a   Zuo, Xian Bo ^a   Cao, Yun Xia ^a   Zhang, Xue Jun ^a  

^a ANHUI MEDICAL UNIVERSITY   (China)

^b UNIVERSITY HOSPITAL ULM   (Germany)

Author keywords

haplotype; male infertility; non obstructive azoospermia; severe oligozoospermia; single nucleotide polymorphism (SNP)

Indexed keywords

PROTAMINE; PROTEIN PROTAMINE1; PROTEIN PROTAMINE2; UNCLASSIFIED DRUG;

ADULT; ARTICLE; AZOOSPERMIA; CHINESE; CONTROLLED STUDY; DISEASE SEVERITY; GENE; GENETIC RISK; GENETIC VARIABILITY; GENOTYPE; HAPLOTYPE; HUMAN; HUMAN TISSUE; KIT GENE; KITLG GENE; MAJOR CLINICAL STUDY; MALE; MALE INFERTILITY; NUCLEOTIDE SEQUENCE; OLIGOSPERMIA; PHENOTYPE; SINGLE NUCLEOTIDE POLYMORPHISM; SPERMATOGENESIS;

ADULT; AMINO ACID SUBSTITUTION; ASIAN CONTINENTAL ANCESTRY GROUP; AZOOSPERMIA; CASE-CONTROL STUDIES; CHINA; GENES, DOMINANT; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; HAPLOTYPES; HUMANS; MALE; OLIGOSPERMIA; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTAMINES; PROTO-ONCOGENE PROTEINS C-KIT; SEVERITY OF ILLNESS INDEX; SPERMATOGENESIS; STEM CELL FACTOR;

EID: 84870482918     PISSN: 14726483     EISSN: 14726491     Source Type: Journal    
DOI: 10.1016/j.rbmo.2012.09.005     Document Type: Article

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