Distribution of gene mutations associated with familial normosmic idiopathic hypogonadotropic hypogonadism

JCRPE Journal of Clinical Research in Pediatric Endocrinology

Volumn 4, Issue 3, 2012, Pages 121-126

  Gürbüz, Fatih ^a   Damla Kotan, L ^b   Mengen, Eda ^a   Şiklar, Zeynep ^c   Berberoǧlu, Merih ^c   Dökmetaş, Sebila ^d   Kiliçli, Mehmet Fatih ^d   Güven, Ayla ^e   Kirel, Birgül ^f   Saka, Nurçin ^g   Poyrazoǧlu, Şükran ^g   Cesur, Yaşar ^h   Doǧan, Murat ^h   Özen, Samim ⁱ   Özbek, Mehmet Nuri ^j   Demirbilek, Hüseyin ^j   Burcu Keki, M ^b   Temiz, Fatih ^a   Mungan, Neslihan Önenli ^a   Yüksel, Bilgin ^a   Topaloǧlu, Ali Kemal ^a,b   more..

^a CUKUROVA UNIVERSITY FACULTY OF MEDICINE   (Turkey)

^b CUKUROVA UNIVERSITY   (Turkey)

^c ANKARA UNIVERSITY   (Turkey)

^d CUMHURIYET UNIVERSITY SCHOOL OF MEDICINE   (Turkey)

^e GOZTEPE TRAINING AND RESEARCH HOSPITAL   (Turkey)

^f OSMANGAZI UNIVERSITY MEDICAL FACULTY   (Turkey)

^g ISTANBUL UNIVERSITY   (Turkey)

^h YUZUNCU YIL UNIVERSITY   (Turkey)

ⁱ Mersin Children's Hospital   (Turkey)

^j Diyarbakir Children Hospital   (Turkey)

more..

Author keywords

Gene; Mutation; Normosmic idiopathic hypogonadotropic hypogonadism

Indexed keywords

FOLLITROPIN; G PROTEIN COUPLED RECEPTOR 54; GONADORELIN RECEPTOR; LUTEINIZING HORMONE; METASTIN; PROTEIN TAC3; PROTEIN TACR3; TACHYKININ; TACHYKININ RECEPTOR; TESTOSTERONE; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CLINICAL ARTICLE; FEMALE; GENE MUTATION; HORMONE BLOOD LEVEL; HUMAN; HYPOGONADOTROPIC HYPOGONADISM; IDIOPATHIC DISEASE; INFANT; MALE; MISSENSE MUTATION; NORMOSMIC IDIOPATHIC HYPOGONADOTROPIC HYPOGONADISM; PHENOTYPE; PRIMARY AMENORRHEA;

ADOLESCENT; ADULT; COHORT STUDIES; FAMILY HEALTH; GENETIC ASSOCIATION STUDIES; HUMANS; HYPOGONADISM; INFANT; KISSPEPTINS; MALE; MUTATION; NEUROKININ B; PROSPECTIVE STUDIES; PROTEIN ISOFORMS; RECEPTORS, G-PROTEIN-COUPLED; RECEPTORS, LHRH; RECEPTORS, NEUROKININ-3; TACHYKININS; TURKEY; YOUNG ADULT;

EID: 84866435612     PISSN: 13085727     EISSN: 13085735     Source Type: Journal    
DOI: 10.4274/Jcrpe.725     Document Type: Article

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