A novel heterozygous deletion frameshift mutation of GATA3 in a Japanese kindred with the hypoparathyroidism, deafness and renal dysplasia syndrome [2]

H. Kobayashi, M. Kasahara, M. Hino, H. Yoshimura, S. Takahara, K. Ikeda, C. Son, T. Iwakura, A. Yoshimoto, T. Ishihara, Y. Ogawa

Research output: Contribution to journalLetter

7 Citations (Scopus)
Original languageEnglish
Pages (from-to)851-853
Number of pages3
JournalJournal of Endocrinological Investigation
Volume29
Issue number9
DOIs
Publication statusPublished - Oct 2006

All Science Journal Classification (ASJC) codes

  • Endocrinology, Diabetes and Metabolism
  • Endocrinology

Cite this

A novel heterozygous deletion frameshift mutation of GATA3 in a Japanese kindred with the hypoparathyroidism, deafness and renal dysplasia syndrome [2]. / Kobayashi, H.; Kasahara, M.; Hino, M.; Yoshimura, H.; Takahara, S.; Ikeda, K.; Son, C.; Iwakura, T.; Yoshimoto, A.; Ishihara, T.; Ogawa, Y.

In: Journal of Endocrinological Investigation, Vol. 29, No. 9, 10.2006, p. 851-853.

Research output: Contribution to journalLetter

Kobayashi, H, Kasahara, M, Hino, M, Yoshimura, H, Takahara, S, Ikeda, K, Son, C, Iwakura, T, Yoshimoto, A, Ishihara, T & Ogawa, Y 2006, 'A novel heterozygous deletion frameshift mutation of GATA3 in a Japanese kindred with the hypoparathyroidism, deafness and renal dysplasia syndrome [2]', Journal of Endocrinological Investigation, vol. 29, no. 9, pp. 851-853. https://doi.org/10.1007/BF03347383
Kobayashi, H. ; Kasahara, M. ; Hino, M. ; Yoshimura, H. ; Takahara, S. ; Ikeda, K. ; Son, C. ; Iwakura, T. ; Yoshimoto, A. ; Ishihara, T. ; Ogawa, Y. / A novel heterozygous deletion frameshift mutation of GATA3 in a Japanese kindred with the hypoparathyroidism, deafness and renal dysplasia syndrome [2]. In: Journal of Endocrinological Investigation. 2006 ; Vol. 29, No. 9. pp. 851-853.
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author = "H. Kobayashi and M. Kasahara and M. Hino and H. Yoshimura and S. Takahara and K. Ikeda and C. Son and T. Iwakura and A. Yoshimoto and T. Ishihara and Y. Ogawa",
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T1 - A novel heterozygous deletion frameshift mutation of GATA3 in a Japanese kindred with the hypoparathyroidism, deafness and renal dysplasia syndrome [2]

AU - Kobayashi, H.

AU - Kasahara, M.

AU - Hino, M.

AU - Yoshimura, H.

AU - Takahara, S.

AU - Ikeda, K.

AU - Son, C.

AU - Iwakura, T.

AU - Yoshimoto, A.

AU - Ishihara, T.

AU - Ogawa, Y.

PY - 2006/10

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