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91938.
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A mutation in Tpst2 encoding tyrosylprotein sulfotransferase causes dwarfism associated with hypothyroidism. [electronic resource] by
- Sasaki, Nobuya
- Hosoda, Yayoi
- Nagata, Aogu
- Ding, Ming
- Cheng, Ji-Ming
- Miyamoto, Tomomi
- Okano, Shinya
- Asano, Atsushi
- Miyoshi, Ichiro
- Agui, Takashi
Producer: 20070815
In:
Molecular endocrinology (Baltimore, Md.) vol. 21
Availability: No items available.
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91939.
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91940.
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A new genetic disorder in mitochondrial fatty acid beta-oxidation: ACAD9 deficiency. [electronic resource] by
- He, M
- Rutledge, S L
- Kelly, D R
- Palmer, C A
- Murdoch, G
- Majumder, N
- Nicholls, R D
- Pei, Z
- Watkins, P A
- Vockley, J
Producer: 20070904
In:
American journal of human genetics vol. 81
Availability: No items available.
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