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

doi:10.1007/BF03347383

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 journal › Letter › peer-review

7 Citations (Scopus)

Original language	English
Pages (from-to)	851-853
Number of pages	3
Journal	Journal of Endocrinological Investigation
Volume	29
Issue number	9
DOIs	https://doi.org/10.1007/BF03347383
Publication status	Published - Oct 2006
Externally published	Yes

All Science Journal Classification (ASJC) codes

Endocrinology, Diabetes and Metabolism
Endocrinology

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This output contributes to the following UN Sustainable Development Goals (SDGs)

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10.1007/BF03347383

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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, 29(9), 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 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

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

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",

year = "2006",

month = oct,

doi = "10.1007/BF03347383",

language = "English",

volume = "29",

pages = "851--853",

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TY - JOUR

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

Y1 - 2006/10

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U2 - 10.1007/BF03347383

DO - 10.1007/BF03347383

M3 - Letter

C2 - 17114920

AN - SCOPUS:33845325332

SN - 0391-4097

VL - 29

SP - 851

EP - 853

JO - Journal of Endocrinological Investigation

JF - Journal of Endocrinological Investigation

IS - 9

ER -

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

All Science Journal Classification (ASJC) codes

UN SDGs

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