Diabetes mellitus, deafness, muscle Weakness and hypocalcemia in a patient with an A3243G mutation of the mitochondrial DNA

Internal Medicine

Volumn 39, Issue 3, 2000, Pages 249-252

  Tanaka, Kiyonobu ^a   Takada, Yasuharu ^a   Matsunaka, Tsuyoshi ^a   Yuyama, Susumu ^a   Fujino, Shun ^a   Maguchi, Motofumi ^a   Yamashita, Shogo ^a   Yuba, Ideo ^a  

^a Saiseikai Saijo Hospital   (Japan)

Author keywords

Hypoparathyroidism; Maternal inheritance; Parathyroid hormone

Indexed keywords

CALCIUM; MITOCHONDRIAL DNA; PARATHYROID HORMONE; PRIMER DNA;

ARTICLE; BLOOD; CASE REPORT; CHEMISTRY; DIABETES MELLITUS; FEMALE; GENETICS; HEARING IMPAIRMENT; HUMAN; HYPOCALCEMIA; HYPOPARATHYROIDISM; MIDDLE AGED; MUSCLE WEAKNESS; NUCLEOTIDE SEQUENCE; PEDIGREE; PHENOTYPE; POINT MUTATION;

CALCIUM; DEAFNESS; DIABETES MELLITUS; DNA MUTATIONAL ANALYSIS; DNA PRIMERS; DNA, MITOCHONDRIAL; FEMALE; HUMANS; HYPOCALCEMIA; HYPOPARATHYROIDISM; MIDDLE AGED; MUSCLE WEAKNESS; PARATHYROID HORMONE; PEDIGREE; PHENOTYPE; POINT MUTATION;

EID: 0034150023     PISSN: 09182918     EISSN: None     Source Type: Journal    
DOI: 10.2169/internalmedicine.39.249     Document Type: Article

References (19)

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