SCOPUS 정보 검색 플랫폼

Volumn 21, Issue 7, 2006, Pages 1056-1057

Barttin mutations in antenatal Bartter syndrome with sensorineural deafness [5]

(8) Ozlu, Ferda a Yapicioǧlu, Hacer a Satar, Mehmet a Narli, Nejat a Ozcan, Kenan a Buyukcelik, Mithat a Konrad, Martin b Demirhan, Osman a

a CUKUROVA UNIVERSITY (Turkey)

b CH (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

CHLORIDE CHANNEL; INDOMETACIN; POTASSIUM; SPIRONOLACTONE;

BARTTER SYNDROME; CASE REPORT; CLINICAL FEATURE; CONSANGUINEOUS MARRIAGE; DRUG DOSE REGIMEN; DRUG WITHDRAWAL; EVOKED BRAIN STEM RESPONSE; GENE MUTATION; GESTATIONAL AGE; HOMOZYGOSITY; HUMAN; HYDRAMNIOS; INFANT; KIDNEY DYSFUNCTION; LETTER; MALE; PERCEPTION DEAFNESS; PHYSICAL EXAMINATION; POTASSIUM BLOOD LEVEL; PRIORITY JOURNAL;

BARTTER SYNDROME; CHLORIDE CHANNELS; HEARING LOSS, SENSORINEURAL; HUMANS; INFANT, NEWBORN; MALE; MEMBRANE PROTEINS; MUTATION;

EID: 33745107464 PISSN: 0931041X EISSN: None Source Type: Journal
DOI: 10.1007/s00467-006-0108-4 Document Type: Letter

Times cited : (12)

References (6)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.