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Uncommon missense and splice mutations and resulting biochemical phenotypes in German patients with X-linked chronic granulomatous disease

✍ Scribed by Joachim Roesler; Stefan Heyden; Martin Burdelski; Hansjorg Schäfer; Hans-Walter Kreth; Romy Lehmann; Diana Paul; Jenny Marzahn; Manfred Gahr; Angela Rösen-Wolff

Book ID: 114217280
Publisher: Elsevier Science
Year: 1999
Tongue: English
Weight: 94 KB
Volume: 27
Category: Article
ISSN: 0301-472X
DOI: 10.1016/s0301-472x(98)00024-1

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