<?xml version="1.0" encoding="UTF-8"?>
<mods xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns="http://www.loc.gov/mods/v3" version="3.1" xsi:schemaLocation="http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-1.xsd">
  <titleInfo>
    <nonSort>The </nonSort>
    <title>metabolic and molecular bases of inherited disease</title>
  </titleInfo>
  <titleInfo type="alternative">
    <title>Metabolic basis of inherited disease</title>
  </titleInfo>
  <name type="personal">
    <namePart>Scriver, Charles R.</namePart>
  </name>
  <typeOfResource>text</typeOfResource>
  <originInfo>
    <place>
      <placeTerm type="text">New York</placeTerm>
    </place>
    <publisher>McGraw-Hill, Health Professions Division</publisher>
    <dateIssued>c1995</dateIssued>
    <edition>7th ed.</edition>
    <issuance>monographic</issuance>
  </originInfo>
  <physicalDescription>
    <form authority="marcform">print</form>
    <extent>3 v. (xxxvi, 4605, 93 p.) : ill. ; 29 cm.</extent>
  </physicalDescription>
  <tableOfContents>V. 1. General themes -- Cancer and genetics -- Chromosomes and autosomes -- Carbohydrates -- Amino acids -- Organic acids -- V. 2. Purines and pyrimidines -- Lipoprotein and lipid metabolism disorders -- Porphyrins and heme -- Metals -- Peroxisomes -- Lysosomal enzymes -- Hormones: synthesis and action -- Vitamins -- V. 3. Blood and blood forming tissue -- Membrane transport systems -- Defense and immune mechanisms -- Connective tissues -- Muscle -- Eye -- Skin -- Intestine -- Neurogenetics -- Significant developments in progress.</tableOfContents>
  <note type="statement of responsibility">editors, Charles R. Scriver ... [et al.] ; consulting editors, John B. Stanbury, James B. Wyngaarden, Donald G. Fredrickson.</note>
  <note>Rev. ed. of: The metabolic basis of inherited disease. 6th ed. c1989.</note>
  <note>Includes bibliographical references.</note>
  <subject authority="lcsh">
    <topic>Metabolism, Inborn errors of</topic>
  </subject>
  <subject authority="lcsh">
    <topic>Medical genetics</topic>
  </subject>
  <subject authority="lcsh">
    <topic>Pathology, Molecular</topic>
  </subject>
  <subject authority="mesh">
    <topic>Hereditary Diseases</topic>
  </subject>
  <subject authority="mesh">
    <topic>Metabolic Diseases</topic>
  </subject>
  <subject authority="mesh">
    <topic>Metabolism, Inborn Errors</topic>
  </subject>
  <classification authority="lcc">MAIN</classification>
  <identifier type="isbn">0070607311 (v. 3 : alk. paper)</identifier>
  <recordInfo>
    <recordContentSource authority="marcorg"/>
    <recordCreationDate encoding="marc">      </recordCreationDate>
    <recordChangeDate encoding="iso8601">20230120203957.0</recordChangeDate>
  </recordInfo>
</mods>
