FMR1 premutation is an uncommon explanation for premature ovarian failure in Han Chinese

PLoS ONE

Volumn 9, Issue 7, 2014, Pages

  Guo, Ting ^a   Qin, Yingying ^a   Jiao, Xue ^a   Li, Guangyu ^a   Simpson, Joe Leigh ^b,c   Chen, Zi Jiang ^a,d  

^a SHANDONG UNIVERSITY   (China)

^b March of Dimes Birth Defects Foundation   (United States)

^c FLORIDA INTERNATIONAL UNIVERSITY   (United States)

^d SHANGHAI JIAO TONG UNIVERSITY SCHOOL OF MEDICINE   (China)

Author keywords

[No Author keywords available]

Indexed keywords

FRAGILE X MENTAL RETARDATION PROTEIN; FMR1 PROTEIN, HUMAN;

ADULT; ALLELE; ARTICLE; CAUCASIAN; CGG REPEAT; COHORT ANALYSIS; CONTROLLED STUDY; FEMALE; FEMALE FERTILITY; FMR1 GENE; GENE FREQUENCY; HAN CHINESE; HUMAN; KARYOTYPE 46,XX; MAJOR CLINICAL STUDY; MENOPAUSE; OVARIAN RESERVE; PREMATURE OVARIAN FAILURE; PREVALENCE; TRINUCLEOTIDE REPEAT; AGING; ASIAN CONTINENTAL ANCESTRY GROUP; CHINA; GENETICS; GENOTYPE; METABOLISM; OVARY; PATHOLOGY; PRIMARY OVARIAN INSUFFICIENCY;

ADULT; AGING; ALLELES; ASIAN CONTINENTAL ANCESTRY GROUP; CHINA; FEMALE; FRAGILE X MENTAL RETARDATION PROTEIN; GENOTYPE; HUMANS; MENOPAUSE; OVARY; PRIMARY OVARIAN INSUFFICIENCY; TRINUCLEOTIDE REPEATS;

EID: 84904656975     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0103316     Document Type: Article

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